UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131513290G= , CM000671.2:g.131513290G= | GRCh38 |
| NC_000009.11:g.134388677G= , CM000671.1:g.134388677G= | GRCh37 |
| NC_000009.10:g.133378498G= | NCBI36 |
| NG_008896.1:g.15389G= | |
| NG_008896.2:g.15389G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000341012.13:c.972G= | ENSP00000343034.7:p.Met324= | |
| ENST00000404875.7:n.1674G= | ||
| ENST00000423007.6:c.1191G= | ENSP00000404119.2:p.Met397= | |
| ENST00000677295.2:c.*1478G= | ENSP00000504346.2:n.*1478G= | |
| ENST00000678264.2:c.*1317G= | ENSP00000503157.2:n.*1317G= | |
| ENST00000682070.1:n.1599G= | ||
| ENST00000682813.1:n.1399G= | ||
| ENST00000683392.1:n.3881G= | ||
| ENST00000683712.1:n.1539G= | ||
| ENST00000683900.1:n.3034G= | ||
| ENST00000684062.1:n.1800G= | ||
| ENST00000684579.1:n.2980G= | ||
| ENST00000341012.12:c.972G= | ENSP00000343034.7:p.Met324= | |
| ENST00000372220.5:c.3G= | ENSP00000361294.5:p.Met1= | |
| ENST00000372228.9:c.1200G= | ENSP00000361302.3:p.Met400= | |
| ENST00000402686.8:c.1134G= MANE Select | ENSP00000385797.4:p.Met378= | |
| ENST00000676640.1:c.1134G= | ENSP00000503281.1:p.Met378= | |
| ENST00000676803.1:c.309G= | ENSP00000503093.1:p.Met103= | |
| ENST00000676835.1:c.*349G= | ENSP00000502911.1:n.*349G= | |
| ENST00000677029.1:c.678G= | ENSP00000502936.1:p.Met226= | |
| ENST00000677099.1:c.*844G= | ENSP00000504553.1:n.*844G= | |
| ENST00000677216.1:c.783G= | ENSP00000503772.1:p.Met261= | |
| ENST00000677293.1:c.309G= | ENSP00000504278.1:p.Met103= | |
| ENST00000677295.1:c.*511G= | ENSP00000504346.1:n.*511G= | |
| ENST00000677444.1:c.940G= | ||
| ENST00000677586.1:n.615G= | ||
| ENST00000677626.1:c.824+1823G= | ENSP00000503552.1:n.824+1823G= | |
| ENST00000677677.1:n.1094G= | ||
| ENST00000677853.1:c.*142G= | ENSP00000503488.1:n.*142G= | |
| ENST00000677944.1:c.396G= | ||
| ENST00000678264.1:c.*511G= | ENSP00000503157.1:n.*511G= | |
| ENST00000678303.1:c.1044G= | ENSP00000503696.1:p.Met348= | |
| ENST00000678366.1:c.*1383G= | ENSP00000504353.1:n.*1383G= | |
| ENST00000678546.1:c.*1079G= | ENSP00000503062.1:n.*1079G= | |
| ENST00000678548.1:c.*1206G= | ENSP00000503934.1:n.*1206G= | |
| ENST00000678626.1:n.831G= | ||
| ENST00000678733.1:c.256+1154G= | ||
| ENST00000678739.1:c.*1460G= | ENSP00000503806.1:n.*1460G= | |
| ENST00000678795.1:n.221G= | ||
| ENST00000678833.1:c.*581G= | ENSP00000503893.1:n.*581G= | |
| ENST00000678942.1:c.314G= | ENSP00000504690.1:n.314G= | |
| ENST00000679023.1:c.972G= | ENSP00000503718.1:p.Met324= | |
| ENST00000679073.1:c.512G= | ENSP00000504356.1:n.512G= | |
| ENST00000679076.1:c.753G= | ||
| ENST00000679111.1:c.1134G= | ENSP00000504257.1:p.Met378= | |
| ENST00000679189.1:c.783G= | ENSP00000503356.1:p.Met261= | |
| ENST00000341012.11:c.972G= | ENSP00000343034.7:p.Met324= | |
| ENST00000372228.7:c.1200G= | ENSP00000361302.3:p.Met400= | |
| ENST00000402686.7:c.1134G= | ENSP00000385797.3:p.Met378= | |
| ENST00000404875.6:c.783G= | ENSP00000384531.2:p.Met261= | |
| ENST00000423007.5:c.1134G= | ENSP00000404119.1:p.Met378= | |
| ENST00000441334.5:c.849G= | ENSP00000395060.1:p.Met283= | |
| ENST00000462375.5:n.960G= | ||
| ENST00000485278.5:n.1689G= | ||
| NM_001077365.1:c.1134G= | NP_001070833.1:p.Met378= | |
| NM_001077366.1:c.972G= | NP_001070834.1:p.Met324= | |
| NM_001136113.1:c.1134G= | NP_001129585.1:p.Met378= | |
| NM_001136114.1:c.783G= | NP_001129586.1:p.Met261= | |
| NM_007171.3:c.1200G= | NP_009102.3:p.Met400= | |
| XM_005272156.1:c.1200G= | XP_005272213.1:p.Met400= | |
| XM_005272158.1:c.1038G= | XP_005272215.1:p.Met346= | |
| XM_005272159.1:c.849G= | XP_005272216.1:p.Met283= | |
| XM_005272162.1:c.3G= | XP_005272219.1:p.Met1= | |
| XM_006716932.1:c.849G= | XP_006716995.1:p.Met283= | |
| XM_011518140.1:c.1053G= | XP_011516442.1:p.Met351= | |
| XM_011518141.1:c.987G= | XP_011516443.1:p.Met329= | |
| XM_011518142.1:c.891G= | XP_011516444.1:p.Met297= | |
| XM_011518143.1:c.885G= | XP_011516445.1:p.Met295= | |
| XM_011518144.1:c.1200G= | XP_011516446.1:p.Met400= | |
| XM_011518145.1:c.744G= | XP_011516447.1:p.Met248= | |
| XM_011518146.1:c.885G= | XP_011516448.1:p.Met295= | |
| XR_929703.1:n.1376G= | ||
| NM_001353193.1:c.1200G= | NP_001340122.1:p.Met400= | |
| NM_001353194.1:c.972G= | NP_001340123.1:p.Met324= | |
| NM_001353195.1:c.783G= | NP_001340124.1:p.Met261= | |
| NM_001353196.1:c.1044G= | NP_001340125.1:p.Met348= | |
| NM_001353197.1:c.1038G= | NP_001340126.1:p.Met346= | |
| NM_001353198.1:c.1038G= | NP_001340127.1:p.Met346= | |
| NM_001353199.1:c.849G= | NP_001340128.1:p.Met283= | |
| NM_001353200.1:c.678G= | NP_001340129.1:p.Met226= | |
| NR_148391.1:n.1184G= | ||
| NR_148392.1:n.1402G= | ||
| NR_148393.1:n.1184G= | ||
| NR_148394.1:n.1077G= | ||
| NR_148395.1:n.1336G= | ||
| NR_148396.1:n.970G= | ||
| NR_148397.1:n.1234G= | ||
| NR_148398.1:n.1189G= | ||
| NR_148399.1:n.1576G= | ||
| NR_148400.1:n.1175G= | ||
| XM_005272162.3:c.3G= | XP_005272219.1:p.Met1= | |
| XM_006716932.2:c.849G= | XP_006716995.1:p.Met283= | |
| XM_011518140.2:c.1053G= | XP_011516442.1:p.Met351= | |
| XM_011518141.2:c.987G= | XP_011516443.1:p.Met329= | |
| XM_011518142.2:c.891G= | XP_011516444.1:p.Met297= | |
| XM_011518143.2:c.885G= | XP_011516445.1:p.Met295= | |
| XM_011518145.2:c.744G= | XP_011516447.1:p.Met248= | |
| XM_017014205.2:c.3G= | XP_016869694.1:p.Met1= | |
| XM_024447380.1:c.3G= | XP_024303148.1:p.Met1= | |
| XM_024447381.1:c.309G= | XP_024303149.1:p.Met103= | |
| XM_024447382.1:c.3G= | XP_024303150.1:p.Met1= | |
| XR_001746160.2:n.1304G= | ||
| XR_001746162.2:n.1370G= | ||
| XR_001746164.1:n.1087G= | ||
| XR_001746166.2:n.1521G= | ||
| NM_001077365.2:c.1134G= MANE Select | NP_001070833.1:p.Met378= | |
| NM_001077366.2:c.972G= | NP_001070834.1:p.Met324= | |
| NM_001136113.2:c.1134G= | NP_001129585.1:p.Met378= | |
| NM_001136114.2:c.783G= | NP_001129586.1:p.Met261= | |
| NM_001353193.2:c.1200G= | NP_001340122.2:p.Met400= | |
| NM_001353194.2:c.972G= | NP_001340123.1:p.Met324= | |
| NM_001353195.2:c.783G= | NP_001340124.1:p.Met261= | |
| NM_001353196.2:c.1044G= | NP_001340125.1:p.Met348= | |
| NM_001353197.2:c.1038G= | NP_001340126.2:p.Met346= | |
| NM_001353198.2:c.1038G= | NP_001340127.2:p.Met346= | |
| NM_001353199.2:c.849G= | NP_001340128.2:p.Met283= | |
| NM_001353200.2:c.678G= | NP_001340129.1:p.Met226= | |
| NM_001374689.1:c.1122G= | NP_001361618.1:p.Met374= | |
| NM_001374690.1:c.1134G= | NP_001361619.1:p.Met378= | |
| NM_001374691.1:c.783G= | NP_001361620.1:p.Met261= | |
| NM_001374692.1:c.783G= | NP_001361621.1:p.Met261= | |
| NM_001374693.1:c.824+1823G= | NP_001361622.1:n.824+1823G= | |
| NM_001374695.1:c.744G= | NP_001361624.1:p.Met248= | |
| NM_007171.4:c.1200G= | NP_009102.4:p.Met400= | |
| NR_148391.2:n.1168G= | ||
| NR_148392.2:n.1386G= | ||
| NR_148393.2:n.1168G= | ||
| NR_148394.2:n.1061G= | ||
| NR_148395.2:n.1320G= | ||
| NR_148396.2:n.954G= | ||
| NR_148397.2:n.1218G= | ||
| NR_148398.2:n.1173G= | ||
| NR_148399.2:n.1560G= | ||
| NR_148400.2:n.1159G= |