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.
Linked Data
gnomAD v4:
7-148807675-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.148807675C>G , CM000669.2:g.148807675C>G | GRCh38 |
| NC_000007.13:g.148504767C>G , CM000669.1:g.148504767C>G | GRCh37 |
| NC_000007.12:g.148135700C>G | NCBI36 |
| NG_032043.1:g.81675G>C , LRG_531:g.81675G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682263.1:n.4127G>C | ||
| ENST00000682317.1:c.*1289G>C | ENSP00000508286.1:n.*1289G>C | |
| ENST00000683292.1:c.*1123G>C | ENSP00000507503.1:n.*1123G>C | |
| ENST00000683293.1:n.3946G>C | ||
| ENST00000683744.1:c.*1289G>C | ENSP00000506949.1:n.*1289G>C | |
| ENST00000684300.1:c.*1289G>C | ENSP00000508407.1:n.*1289G>C | |
| ENST00000684400.1:n.4214G>C | ||
| ENST00000684436.1:n.2543G>C | ||
| ENST00000684510.1:n.2605G>C | ||
| ENST00000320356.7:c.2227G>C MANE Select | ENSP00000320147.2:p.Gly743Arg | |
| ENST00000320356.6:c.2227G>C | ENSP00000320147.2:p.Gly743Arg | |
| ENST00000350995.6:c.2095G>C | ENSP00000223193.2:p.Gly699Arg | |
| ENST00000460911.5:c.2212G>C | ENSP00000419711.1:p.Gly738Arg | |
| ENST00000476773.5:c.2059G>C | ENSP00000419050.1:p.Gly687Arg | |
| ENST00000478654.5:c.2059G>C | ENSP00000417062.1:p.Gly687Arg | |
| ENST00000483967.5:c.2185G>C | ENSP00000419856.1:p.Gly729Arg | |
| ENST00000492143.5:c.*2217G>C | ENSP00000417377.1:n.*2217G>C | |
| NM_001203247.1:c.2212G>C | NP_001190176.1:p.Gly738Arg | |
| NM_001203248.1:c.2185G>C | NP_001190177.1:p.Gly729Arg | |
| NM_001203249.1:c.2059G>C | NP_001190178.1:p.Gly687Arg | |
| NM_004456.4:c.2227G>C , LRG_531t1:c.2227G>C | NP_004447.2:p.Gly743Arg | |
| NM_152998.2:c.2095G>C | NP_694543.1:p.Gly699Arg | |
| XM_005249962.3:c.2236G>C | XP_005250019.1:p.Gly746Arg | |
| XM_005249963.3:c.2209G>C | XP_005250020.1:p.Gly737Arg | |
| XM_005249964.3:c.2083G>C | XP_005250021.1:p.Gly695Arg | |
| XM_011515883.1:c.2251G>C | XP_011514185.1:p.Gly751Arg | |
| XM_011515884.1:c.2227G>C | XP_011514186.1:p.Gly743Arg | |
| XM_011515885.1:c.2224G>C | XP_011514187.1:p.Gly742Arg | |
| XM_011515886.1:c.2203G>C | XP_011514188.1:p.Gly735Arg | |
| XM_011515887.1:c.2200G>C | XP_011514189.1:p.Gly734Arg | |
| XM_011515888.1:c.2200G>C | XP_011514190.1:p.Gly734Arg | |
| XM_011515889.1:c.2161G>C | XP_011514191.1:p.Gly721Arg | |
| XM_011515890.1:c.2134G>C | XP_011514192.1:p.Gly712Arg | |
| XM_011515891.1:c.2128G>C | XP_011514193.1:p.Gly710Arg | |
| XM_011515892.1:c.2125G>C | XP_011514194.1:p.Gly709Arg | |
| XM_011515893.1:c.2119G>C | XP_011514195.1:p.Gly707Arg | |
| XM_011515894.1:c.2110G>C | XP_011514196.1:p.Gly704Arg | |
| XM_011515895.1:c.2107G>C | XP_011514197.1:p.Gly703Arg | |
| XM_011515896.1:c.1993G>C | XP_011514198.1:p.Gly665Arg | |
| XM_011515897.1:c.1900G>C | XP_011514199.1:p.Gly634Arg | |
| XM_011515898.1:c.1900G>C | XP_011514200.1:p.Gly634Arg | |
| XR_928101.1:n.515+2590C>G | ||
| XR_928102.1:n.722+2590C>G | ||
| XM_005249962.4:c.2236G>C | XP_005250019.1:p.Gly746Arg | |
| XM_005249963.4:c.2209G>C | XP_005250020.1:p.Gly737Arg | |
| XM_005249964.4:c.2083G>C | XP_005250021.1:p.Gly695Arg | |
| XM_011515883.2:c.2251G>C | XP_011514185.1:p.Gly751Arg | |
| XM_011515884.2:c.2227G>C | XP_011514186.1:p.Gly743Arg | |
| XM_011515885.2:c.2224G>C | XP_011514187.1:p.Gly742Arg | |
| XM_011515886.2:c.2203G>C | XP_011514188.1:p.Gly735Arg | |
| XM_011515887.3:c.2200G>C | XP_011514189.1:p.Gly734Arg | |
| XM_011515888.2:c.2200G>C | XP_011514190.1:p.Gly734Arg | |
| XM_011515889.2:c.2161G>C | XP_011514191.1:p.Gly721Arg | |
| XM_011515890.2:c.2134G>C | XP_011514192.1:p.Gly712Arg | |
| XM_011515891.3:c.2128G>C | XP_011514193.1:p.Gly710Arg | |
| XM_011515892.2:c.2125G>C | XP_011514194.1:p.Gly709Arg | |
| XM_011515893.2:c.2119G>C | XP_011514195.1:p.Gly707Arg | |
| XM_011515894.2:c.2110G>C | XP_011514196.1:p.Gly704Arg | |
| XM_011515895.2:c.2107G>C | XP_011514197.1:p.Gly703Arg | |
| XM_011515896.2:c.1993G>C | XP_011514198.1:p.Gly665Arg | |
| XM_011515897.2:c.1900G>C | XP_011514199.1:p.Gly634Arg | |
| XM_011515898.2:c.1900G>C | XP_011514200.1:p.Gly634Arg | |
| XM_017011817.2:c.2251G>C | XP_016867306.1:p.Gly751Arg | |
| XM_017011818.1:c.2188G>C | XP_016867307.1:p.Gly730Arg | |
| XM_017011819.1:c.2110G>C | XP_016867308.1:p.Gly704Arg | |
| XM_017011820.2:c.2083G>C | XP_016867309.1:p.Gly695Arg | |
| XM_017011821.1:c.1885G>C | XP_016867310.1:p.Gly629Arg | |
| XM_024446680.1:c.2113G>C | XP_024302448.1:p.Gly705Arg | |
| XR_001744581.1:n.4601G>C | ||
| XR_002956413.1:n.5257G>C | ||
| XR_002956414.1:n.5717G>C | ||
| NM_001203247.2:c.2212G>C | NP_001190176.1:p.Gly738Arg | |
| NM_001203248.2:c.2185G>C | NP_001190177.1:p.Gly729Arg | |
| NM_001203249.2:c.2059G>C | NP_001190178.1:p.Gly687Arg | |
| NM_004456.5:c.2227G>C MANE Select | NP_004447.2:p.Gly743Arg | |
| NM_152998.3:c.2095G>C | NP_694543.1:p.Gly699Arg |