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
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152141203C>T , CM000668.2:g.152141203C>T | GRCh38 |
| NC_000006.11:g.152462338C>T , CM000668.1:g.152462338C>T | GRCh37 |
| NC_000006.10:g.152504031C>T | NCBI36 |
| NG_012855.1:g.501197G>A | |
| NG_012855.2:g.501197G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354674.5:c.1780G>A MANE Plus Clinical | ENSP00000346701.4:p.Gly594Ser | |
| ENST00000367255.10:c.25246G>A MANE Select | ENSP00000356224.5:p.Gly8416Ser | |
| ENST00000423061.6:c.25102G>A | ENSP00000396024.1:p.Gly8368Ser | |
| ENST00000672154.1:c.648G>A | ||
| ENST00000672169.1:c.981G>A | ||
| ENST00000673173.1:c.891-1042G>A | ||
| ENST00000673451.1:c.1018G>A | ENSP00000500189.1:p.Gly340Ser | |
| ENST00000341594.9:c.24031G>A | ENSP00000341887.6:p.Gly8011Ser | |
| ENST00000347037.9:n.1994G>A | ||
| ENST00000354674.4:c.1780G>A | ENSP00000346701.4:p.Gly594Ser | |
| ENST00000367251.7:c.4081G>A | ENSP00000356220.3:p.Gly1361Ser | |
| ENST00000367255.9:c.25246G>A | ENSP00000356224.5:p.Gly8416Ser | |
| ENST00000367256.9:n.8938G>A | ||
| ENST00000367257.8:c.3184G>A | ENSP00000356226.4:p.Gly1062Ser | |
| ENST00000409694.6:n.8830G>A | ||
| ENST00000423061.5:c.25102G>A | ENSP00000396024.1:p.Gly8368Ser | |
| ENST00000460912.6:n.1860G>A | ||
| ENST00000478916.5:n.4268G>A | ||
| ENST00000536990.5:n.2083G>A | ||
| ENST00000539504.5:c.1711G>A | ENSP00000441052.1:p.Gly571Ser | |
| NM_033071.3:c.25102G>A | NP_149062.1:p.Gly8368Ser | |
| NM_182961.3:c.25246G>A | NP_892006.3:p.Gly8416Ser | |
| XM_006715407.1:c.25351G>A | XP_006715470.1:p.Gly8451Ser | |
| XM_006715408.1:c.25339G>A | XP_006715471.1:p.Gly8447Ser | |
| XM_006715409.1:c.25330G>A | XP_006715472.1:p.Gly8444Ser | |
| XM_006715410.1:c.25351G>A | XP_006715473.1:p.Gly8451Ser | |
| XM_006715411.1:c.25300G>A | XP_006715474.1:p.Gly8434Ser | |
| XM_006715412.1:c.25336G>A | XP_006715475.1:p.Gly8446Ser | |
| XM_006715413.1:c.25282G>A | XP_006715476.1:p.Gly8428Ser | |
| XM_006715414.1:c.25279G>A | XP_006715477.1:p.Gly8427Ser | |
| XM_006715415.1:c.25282G>A | XP_006715478.1:p.Gly8428Ser | |
| XM_006715416.1:c.25267G>A | XP_006715479.1:p.Gly8423Ser | |
| XM_006715417.1:c.25210G>A | XP_006715480.1:p.Gly8404Ser | |
| XM_006715420.1:c.25198G>A | XP_006715483.1:p.Gly8400Ser | |
| XM_006715421.1:c.25195G>A | XP_006715484.1:p.Gly8399Ser | |
| XM_006715422.1:c.25192G>A | XP_006715485.1:p.Gly8398Ser | |
| XM_006715423.1:c.25351G>A | XP_006715486.1:p.Gly8451Ser | |
| XM_006715424.1:c.25351G>A | XP_006715487.1:p.Gly8451Ser | |
| XM_006715425.1:c.25282G>A | XP_006715488.1:p.Gly8428Ser | |
| XM_011535641.1:c.25348G>A | XP_011533943.1:p.Gly8450Ser | |
| XM_011535642.1:c.25336G>A | XP_011533944.1:p.Gly8446Ser | |
| XM_011535643.1:c.25186G>A | XP_011533945.1:p.Gly8396Ser | |
| XM_011535644.1:c.23626G>A | XP_011533946.1:p.Gly7876Ser | |
| XM_011535645.1:c.23119G>A | XP_011533947.1:p.Gly7707Ser | |
| XM_011535647.1:c.18586G>A | XP_011533949.1:p.Gly6196Ser | |
| NM_001347701.1:c.1852G>A | NP_001334630.1:p.Gly618Ser | |
| NM_001347702.1:c.1780G>A | NP_001334631.1:p.Gly594Ser | |
| XM_006715408.2:c.25339G>A | XP_006715471.1:p.Gly8447Ser | |
| XM_006715410.2:c.25351G>A | XP_006715473.1:p.Gly8451Ser | |
| XM_006715412.2:c.25336G>A | XP_006715475.1:p.Gly8446Ser | |
| XM_006715413.2:c.25282G>A | XP_006715476.1:p.Gly8428Ser | |
| XM_006715415.2:c.25282G>A | XP_006715478.1:p.Gly8428Ser | |
| XM_006715416.2:c.25267G>A | XP_006715479.1:p.Gly8423Ser | |
| XM_006715417.2:c.25210G>A | XP_006715480.1:p.Gly8404Ser | |
| XM_006715420.2:c.25198G>A | XP_006715483.1:p.Gly8400Ser | |
| XM_006715421.2:c.25195G>A | XP_006715484.1:p.Gly8399Ser | |
| XM_006715423.2:c.25351G>A | XP_006715486.1:p.Gly8451Ser | |
| XM_006715424.2:c.25351G>A | XP_006715487.1:p.Gly8451Ser | |
| XM_006715425.2:c.25282G>A | XP_006715488.1:p.Gly8428Ser | |
| XM_011535641.2:c.25348G>A | XP_011533943.1:p.Gly8450Ser | |
| XM_011535642.2:c.25336G>A | XP_011533944.1:p.Gly8446Ser | |
| XM_011535645.2:c.23119G>A | XP_011533947.1:p.Gly7707Ser | |
| XM_017010608.1:c.25351G>A | XP_016866097.1:p.Gly8451Ser | |
| XM_017010609.1:c.25351G>A | XP_016866098.1:p.Gly8451Ser | |
| XM_017010610.1:c.25330G>A | XP_016866099.1:p.Gly8444Ser | |
| XM_017010611.2:c.25324G>A | XP_016866100.1:p.Gly8442Ser | |
| XM_017010612.1:c.25273G>A | XP_016866101.1:p.Gly8425Ser | |
| XM_017010613.1:c.25279G>A | XP_016866102.1:p.Gly8427Ser | |
| XM_017010614.1:c.25195G>A | XP_016866103.1:p.Gly8399Ser | |
| XM_017010615.1:c.25126G>A | XP_016866104.1:p.Gly8376Ser | |
| XM_017010616.1:c.25282G>A | XP_016866105.1:p.Gly8428Ser | |
| XM_017010617.1:c.25279G>A | XP_016866106.1:p.Gly8427Ser | |
| XM_017010618.1:c.25267G>A | XP_016866107.1:p.Gly8423Ser | |
| XM_017010619.1:c.23626G>A | XP_016866108.1:p.Gly7876Ser | |
| NM_182961.4:c.25246G>A MANE Select | NP_892006.3:p.Gly8416Ser | |
| NM_001347701.2:c.1852G>A | NP_001334630.1:p.Gly618Ser | |
| NM_001347702.2:c.1780G>A MANE Plus Clinical | NP_001334631.1:p.Gly594Ser | |
| NM_033071.5:c.25102G>A | NP_149062.2:p.Gly8368Ser |