Linked Data
ClinVar Variation Id:
694273
dbSNP Id:
rs751511532
ExAC:
4:120188514 C / T
gnomAD v2:
4-120188514-C-T
gnomAD v3:
4-119267359-C-T
gnomAD v4:
4-119267359-C-T
COSMIC:
COSM3008026
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.119267359C>T , CM000666.2:g.119267359C>T | GRCh38 |
| NC_000004.11:g.120188514C>T , CM000666.1:g.120188514C>T | GRCh37 |
| NC_000004.10:g.120407962C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274030.11:c.1012C>T | ENSP00000274030.6:p.Arg338Ter | |
| ENST00000450251.6:c.1012C>T | ENSP00000409906.1:p.Arg338Ter | |
| ENST00000688980.1:c.1012C>T | ENSP00000509357.1:p.Arg338Ter | |
| ENST00000692078.1:c.1012C>T MANE Select | ENSP00000509606.1:p.Arg338Ter | |
| ENST00000274030.10:c.1012C>T | ENSP00000274030.5:p.Arg338Ter | |
| ENST00000450251.5:c.1012C>T | ENSP00000409906.1:p.Arg338Ter | |
| ENST00000507906.5:c.112C>T | ENSP00000421729.1:p.Arg38Ter | |
| ENST00000509769.5:c.*62C>T | ENSP00000426628.1:n.*62C>T | |
| NM_019050.2:c.1012C>T | NP_061923.2:p.Arg338Ter | |
| XM_005263073.2:c.1012C>T | XP_005263130.1:p.Arg338Ter | |
| XM_005263074.3:c.1012C>T | XP_005263131.1:p.Arg338Ter | |
| XM_005263075.1:c.862C>T | XP_005263132.1:p.Arg288Ter | |
| XM_005263076.1:c.1012C>T | XP_005263133.1:p.Arg338Ter | |
| XM_005263077.2:c.1012C>T | XP_005263134.1:p.Arg338Ter | |
| XM_005263078.2:c.1012C>T | XP_005263135.1:p.Arg338Ter | |
| XM_006714240.1:c.664C>T | XP_006714303.1:p.Arg222Ter | |
| XM_011532037.1:c.1012C>T | XP_011530339.1:p.Arg338Ter | |
| XM_011532038.1:c.664C>T | XP_011530340.1:p.Arg222Ter | |
| XM_005263073.4:c.1012C>T | XP_005263130.1:p.Arg338Ter | |
| XM_005263075.3:c.862C>T | XP_005263132.1:p.Arg288Ter | |
| XM_005263076.3:c.1012C>T | XP_005263133.1:p.Arg338Ter | |
| XM_005263077.4:c.1012C>T | XP_005263134.1:p.Arg338Ter | |
| XM_011532037.2:c.1012C>T | XP_011530339.1:p.Arg338Ter | |
| XM_011532038.2:c.664C>T | XP_011530340.1:p.Arg222Ter | |
| XM_017008312.2:c.1012C>T | XP_016863801.1:p.Arg338Ter | |
| XM_017008313.1:c.1012C>T | XP_016863802.1:p.Arg338Ter | |
| XM_017008314.1:c.1012C>T | XP_016863803.1:p.Arg338Ter | |
| XM_017008315.2:c.1012C>T | XP_016863804.1:p.Arg338Ter | |
| XM_017008316.2:c.1012C>T | XP_016863805.1:p.Arg338Ter | |
| XM_017008317.2:c.1012C>T | XP_016863806.1:p.Arg338Ter | |
| XM_017008318.2:c.1012C>T | XP_016863807.1:p.Arg338Ter | |
| NM_001371395.1:c.1012C>T MANE Select | NP_001358324.1:p.Arg338Ter | |
| NM_001371396.1:c.1012C>T | NP_001358325.1:p.Arg338Ter | |
| NM_001371397.1:c.1012C>T | NP_001358326.1:p.Arg338Ter | |
| NM_001371398.1:c.1012C>T | NP_001358327.1:p.Arg338Ter | |
| NM_001371399.1:c.1012C>T | NP_001358328.1:p.Arg338Ter | |
| NM_001389658.1:c.1012C>T | NP_001376587.1:p.Arg338Ter | |
| NM_001389659.1:c.1012C>T | NP_001376588.1:p.Arg338Ter | |
| NM_001389660.1:c.862C>T | NP_001376589.1:p.Arg288Ter | |
| NM_001389661.1:c.1012C>T | NP_001376590.1:p.Arg338Ter | |
| NM_001389662.1:c.664C>T | NP_001376591.1:p.Arg222Ter | |
| NM_001389663.1:c.664C>T | NP_001376592.1:p.Arg222Ter | |
| NM_001389664.1:c.664C>T | NP_001376593.1:p.Arg222Ter | |
| NM_001389665.1:c.664C>T | NP_001376594.1:p.Arg222Ter | |
| NM_001389666.1:c.664C>T | NP_001376595.1:p.Arg222Ter | |
| NM_001389667.1:c.664C>T | NP_001376596.1:p.Arg222Ter | |
| NM_019050.3:c.1012C>T | NP_061923.2:p.Arg338Ter |