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_000001.11:g.45332772T= , CM000663.2:g.45332772T= | GRCh38 |
| NC_000001.10:g.45798444T= , CM000663.1:g.45798444T= | GRCh37 |
| NC_000001.9:g.45571031T= | NCBI36 |
| NG_008189.1:g.12699A= , LRG_220:g.12699A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000412971.6:c.99A= | ENSP00000410263.2:p.Gly33= | |
| ENST00000435155.2:c.516A= | ENSP00000403655.2:p.Gly172= | |
| ENST00000467459.6:c.483A= | ENSP00000435889.2:p.Gly161= | |
| ENST00000483127.2:c.501A= | ENSP00000436469.2:p.Gly167= | |
| ENST00000485271.6:c.483A= | ENSP00000431264.2:p.Gly161= | |
| ENST00000529892.6:c.525A= | ENSP00000432528.2:p.Gly175= | |
| ENST00000533178.6:c.116-85A= | ENSP00000436430.2:n.116-85A= | |
| ENST00000672314.2:c.483A= | ENSP00000500828.2:p.Gly161= | |
| ENST00000674679.2:c.*395A= | ENSP00000501623.2:n.*395A= | |
| ENST00000710952.2:c.567A= MANE Plus Clinical | ENSP00000518552.2:p.Gly189= | |
| ENST00000672818.3:c.558A= | ENSP00000500891.1:p.Gly186= | |
| ENST00000450313.6:c.493A= | ENSP00000408176.2:p.Ser165= | |
| ENST00000456914.7:c.483A= MANE Select | ENSP00000407590.2:p.Gly161= | |
| ENST00000461495.6:c.*222A= | ENSP00000437166.1:n.*222A= | |
| ENST00000671856.1:n.429A= | ||
| ENST00000671898.1:c.1071A= | ENSP00000499896.1:p.Gly357= | |
| ENST00000672011.1:c.451A= | ENSP00000500418.1:p.Ser151= | |
| ENST00000672314.1:c.483A= | ENSP00000500828.1:p.Gly161= | |
| ENST00000672593.1:c.*296A= | ENSP00000500455.1:n.*296A= | |
| ENST00000672764.1:c.442A= | ENSP00000500886.1:p.Ser148= | |
| ENST00000672818.2:c.558A= | ENSP00000500891.1:p.Gly186= | |
| ENST00000673134.1:c.*180A= | ENSP00000500526.1:n.*180A= | |
| ENST00000674679.1:c.511A= | ENSP00000501623.1:n.511A= | |
| ENST00000354383.10:c.486A= | ENSP00000346354.6:p.Gly162= | |
| ENST00000355498.6:c.483A= | ENSP00000347685.2:p.Gly161= | |
| ENST00000372098.7:c.558A= | ENSP00000361170.3:p.Gly186= | |
| ENST00000372104.5:c.483A= | ENSP00000361176.1:p.Gly161= | |
| ENST00000372110.7:c.528A= | ENSP00000361182.3:p.Gly176= | |
| ENST00000372115.7:c.525A= | ENSP00000361187.3:p.Gly175= | |
| ENST00000412971.5:c.99A= | ENSP00000410263.1:p.Gly33= | |
| ENST00000435155.1:c.516A= | ENSP00000403655.1:p.Gly172= | |
| ENST00000448481.5:c.516A= | ENSP00000409718.1:p.Gly172= | |
| ENST00000450313.5:c.567A= | ENSP00000408176.1:p.Gly189= | |
| ENST00000456914.6:c.483A= | ENSP00000407590.2:p.Gly161= | |
| ENST00000461495.5:c.*222A= | ENSP00000437166.1:n.*222A= | |
| ENST00000462388.5:n.174A= | ||
| ENST00000467940.5:c.*406A= | ENSP00000436478.1:n.*406A= | |
| ENST00000470256.5:c.370A= | ENSP00000434985.1:p.Ser124= | |
| ENST00000475516.5:c.*296A= | ENSP00000433843.1:n.*296A= | |
| ENST00000476789.5:n.923A= | ||
| ENST00000478796.5:n.470A= | ||
| ENST00000479746.6:n.766A= | ||
| ENST00000481139.5:n.956A= | ||
| ENST00000481571.5:c.*296A= | ENSP00000436597.1:n.*296A= | |
| ENST00000483642.5:n.998A= | ||
| ENST00000485484.5:n.784A= | ||
| ENST00000488731.6:c.178A= | ENSP00000432330.1:p.Ser60= | |
| ENST00000492494.5:n.880A= | ||
| ENST00000525160.5:c.*134A= | ENSP00000431568.1:n.*134A= | |
| ENST00000528013.6:c.525A= | ENSP00000433130.2:p.Gly175= | |
| ENST00000529984.5:c.178A= | ENSP00000437093.1:p.Ser60= | |
| ENST00000531105.5:c.115+1619A= | ENSP00000431292.1:n.115+1619A= | |
| ENST00000533178.5:c.122-85A= | ENSP00000436430.1:n.122-85A= | |
| NM_001048171.1:c.525A= | NP_001041636.1:p.Gly175= | |
| NM_001048172.1:c.486A= | NP_001041637.1:p.Gly162= | |
| NM_001048173.1:c.483A= | NP_001041638.1:p.Gly161= | |
| NM_001048174.1:c.483A= | NP_001041639.1:p.Gly161= | |
| NM_001128425.1:c.567A= , LRG_220t1:c.567A= | NP_001121897.1:p.Gly189= | |
| NM_001293190.1:c.528A= | NP_001280119.1:p.Gly176= | |
| NM_001293191.1:c.516A= | NP_001280120.1:p.Gly172= | |
| NM_001293192.1:c.207A= | NP_001280121.1:p.Gly69= | |
| NM_001293195.1:c.483A= | NP_001280124.1:p.Gly161= | |
| NM_001293196.1:c.207A= | NP_001280125.1:p.Gly69= | |
| NM_012222.2:c.558A= | NP_036354.1:p.Gly186= | |
| XM_011541497.1:c.543A= | XP_011539799.1:p.Gly181= | |
| XM_011541498.1:c.525A= | XP_011539800.1:p.Gly175= | |
| XM_011541499.1:c.525A= | XP_011539801.1:p.Gly175= | |
| XM_011541500.1:c.525A= | XP_011539802.1:p.Gly175= | |
| XM_011541501.1:c.525A= | XP_011539803.1:p.Gly175= | |
| XM_011541502.1:c.525A= | XP_011539804.1:p.Gly175= | |
| XM_011541503.1:c.525A= | XP_011539805.1:p.Gly175= | |
| XM_011541504.1:c.516A= | XP_011539806.1:p.Gly172= | |
| XM_011541505.1:c.105A= | XP_011539807.1:p.Gly35= | |
| XM_011541506.1:c.105A= | XP_011539808.1:p.Gly35= | |
| XM_011541507.1:c.96A= | XP_011539809.1:p.Gly32= | |
| XM_011541508.1:c.111A= | XP_011539810.1:p.Gly37= | |
| XR_946658.1:n.614A= | ||
| NM_001350650.1:c.138A= | NP_001337579.1:p.Gly46= | |
| NM_001350651.1:c.138A= | NP_001337580.1:p.Gly46= | |
| NR_146882.1:n.741A= | ||
| NR_146883.1:n.555A= | ||
| XM_011541497.3:c.543A= | XP_011539799.1:p.Gly181= | |
| XM_011541500.3:c.525A= | XP_011539802.1:p.Gly175= | |
| XM_011541501.2:c.525A= | XP_011539803.1:p.Gly175= | |
| XM_011541502.2:c.525A= | XP_011539804.1:p.Gly175= | |
| XM_011541503.2:c.525A= | XP_011539805.1:p.Gly175= | |
| XM_011541504.2:c.516A= | XP_011539806.1:p.Gly172= | |
| XM_011541505.2:c.105A= | XP_011539807.1:p.Gly35= | |
| XM_011541506.2:c.105A= | XP_011539808.1:p.Gly35= | |
| XM_017001331.1:c.525A= | XP_016856820.1:p.Gly175= | |
| XM_017001332.1:c.525A= | XP_016856821.1:p.Gly175= | |
| XM_017001333.1:c.525A= | XP_016856822.1:p.Gly175= | |
| XM_017001334.1:c.486A= | XP_016856823.1:p.Gly162= | |
| XM_017001335.1:c.207A= | XP_016856824.1:p.Gly69= | |
| XM_017001336.1:c.138A= | XP_016856825.1:p.Gly46= | |
| XM_017001337.1:c.138A= | XP_016856826.1:p.Gly46= | |
| XM_024447244.1:c.138A= | XP_024303012.1:p.Gly46= | |
| XM_024447245.1:c.138A= | XP_024303013.1:p.Gly46= | |
| XM_024447248.1:c.96A= | XP_024303016.1:p.Gly32= | |
| XM_024447249.1:c.-34A= | XP_024303017.1:n.-34A= | |
| XM_024447250.1:c.-34A= | XP_024303018.1:n.-34A= | |
| XM_024447251.1:c.-34A= | XP_024303019.1:n.-34A= | |
| XR_001737190.1:n.528A= | ||
| XR_001737192.1:n.340A= | ||
| XR_002956643.1:n.520A= | ||
| XR_002956644.1:n.1055A= | ||
| XR_946658.2:n.628A= | ||
| NM_001048171.2:c.483A= | NP_001041636.2:p.Gly161= | |
| NM_001128425.2:c.567A= MANE Plus Clinical | NP_001121897.1:p.Gly189= | |
| NM_001048172.2:c.486A= | NP_001041637.1:p.Gly162= | |
| NM_001048173.2:c.483A= | NP_001041638.1:p.Gly161= | |
| NM_001048174.2:c.483A= MANE Select | NP_001041639.1:p.Gly161= | |
| NM_001293190.2:c.528A= | NP_001280119.1:p.Gly176= | |
| NM_001293191.2:c.516A= | NP_001280120.1:p.Gly172= | |
| NM_001293192.2:c.207A= | NP_001280121.1:p.Gly69= | |
| NM_001293195.2:c.483A= | NP_001280124.1:p.Gly161= | |
| NM_001293196.2:c.207A= | NP_001280125.1:p.Gly69= | |
| NM_001350650.2:c.138A= | NP_001337579.1:p.Gly46= | |
| NM_001350651.2:c.138A= | NP_001337580.1:p.Gly46= | |
| NM_012222.3:c.558A= | NP_036354.1:p.Gly186= | |
| NR_146882.2:n.711A= | ||
| NR_146883.2:n.560A= |