Linked Data
ClinVar Variation Id:
425255
dbSNP Id:
rs1064797281
gnomAD v2:
2-202591411-C-T
gnomAD v3:
2-201726688-C-T
gnomAD v4:
2-201726688-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.201726688C>T , CM000664.2:g.201726688C>T | GRCh38 |
| NC_000002.11:g.202591411C>T , CM000664.1:g.202591411C>T | GRCh37 |
| NC_000002.10:g.202299656C>T | NCBI36 |
| NG_008775.1:g.59485G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264276.11:c.3158G>A MANE Select | ENSP00000264276.6:p.Trp1053Ter | |
| ENST00000439495.6:c.836G>A | ENSP00000403832.2:p.Trp279Ter | |
| ENST00000482891.6:n.3926G>A | ||
| ENST00000494017.6:n.890G>A | ||
| ENST00000679409.1:c.836G>A | ENSP00000506531.1:p.Trp279Ter | |
| ENST00000679416.1:n.4662G>A | ||
| ENST00000679435.1:c.3158G>A | ENSP00000505218.1:p.Trp1053Ter | |
| ENST00000679516.1:c.3158G>A | ENSP00000505187.1:p.Trp1053Ter | |
| ENST00000679618.1:c.*246G>A | ENSP00000506274.1:n.*246G>A | |
| ENST00000679630.1:n.5007G>A | ||
| ENST00000679686.1:n.3272G>A | ||
| ENST00000679701.1:n.5007G>A | ||
| ENST00000679916.1:c.3158G>A | ENSP00000506172.1:p.Trp1053Ter | |
| ENST00000680000.1:c.3158G>A | ENSP00000506173.1:p.Trp1053Ter | |
| ENST00000680135.1:c.*1122G>A | ENSP00000506211.1:n.*1122G>A | |
| ENST00000680149.1:c.3158G>A | ENSP00000506497.1:p.Trp1053Ter | |
| ENST00000680163.1:c.3158G>A | ENSP00000505092.1:p.Trp1053Ter | |
| ENST00000680174.1:n.3849G>A | ||
| ENST00000680236.1:c.*219G>A | ENSP00000506212.1:n.*219G>A | |
| ENST00000680497.1:c.3260G>A | ENSP00000505954.1:p.Trp1087Ter | |
| ENST00000680508.1:c.3158G>A | ENSP00000505749.1:p.Trp1053Ter | |
| ENST00000680569.1:c.*869G>A | ENSP00000505522.1:n.*869G>A | |
| ENST00000680630.1:n.3590G>A | ||
| ENST00000680634.1:n.21-6199G>A | ||
| ENST00000680722.1:n.958G>A | ||
| ENST00000680723.1:n.2798G>A | ||
| ENST00000680726.1:c.3158G>A | ENSP00000505505.1:p.Trp1053Ter | |
| ENST00000680737.1:n.3429G>A | ||
| ENST00000680759.1:c.3158G>A | ENSP00000505848.1:p.Trp1053Ter | |
| ENST00000680814.1:c.3158G>A | ENSP00000505710.1:p.Trp1053Ter | |
| ENST00000680828.1:c.*730G>A | ENSP00000505249.1:n.*730G>A | |
| ENST00000680861.1:c.3158G>A | ENSP00000505043.1:p.Trp1053Ter | |
| ENST00000680927.1:c.3158G>A | ENSP00000505473.1:p.Trp1053Ter | |
| ENST00000680939.1:n.3500G>A | ||
| ENST00000681152.1:c.3158G>A | ENSP00000505388.1:p.Trp1053Ter | |
| ENST00000681250.1:c.1472-1234G>A | ENSP00000505684.1:n.1472-1234G>A | |
| ENST00000681256.1:c.*1176G>A | ENSP00000505446.1:n.*1176G>A | |
| ENST00000681279.1:n.3926G>A | ||
| ENST00000681303.1:c.3158G>A | ENSP00000505576.1:p.Trp1053Ter | |
| ENST00000681307.1:n.4271G>A | ||
| ENST00000681461.1:n.3926G>A | ||
| ENST00000681495.1:c.698G>A | ENSP00000506085.1:p.Trp233Ter | |
| ENST00000681558.1:c.836G>A | ENSP00000505568.1:p.Trp279Ter | |
| ENST00000681619.1:c.3158G>A | ENSP00000505071.1:p.Trp1053Ter | |
| ENST00000681716.1:c.*869G>A | ENSP00000505078.1:n.*869G>A | |
| ENST00000681758.1:n.3500G>A | ||
| ENST00000681768.1:c.*822G>A | ENSP00000506311.1:n.*822G>A | |
| ENST00000681808.1:c.3158G>A | ENSP00000505219.1:p.Trp1053Ter | |
| ENST00000264276.10:c.3158G>A | ENSP00000264276.6:p.Trp1053Ter | |
| ENST00000439495.5:c.1119G>A | ||
| ENST00000482891.5:n.3298G>A | ||
| NM_020919.3:c.3158G>A | NP_065970.2:p.Trp1053Ter | |
| XM_005246709.2:c.3158G>A | XP_005246766.1:p.Trp1053Ter | |
| XM_006712654.1:c.3158G>A | XP_006712717.1:p.Trp1053Ter | |
| XM_006712655.2:c.1094G>A | XP_006712718.1:p.Trp365Ter | |
| XM_011511530.1:c.2819G>A | XP_011509832.1:p.Trp940Ter | |
| XM_011511531.1:c.3158G>A | XP_011509833.1:p.Trp1053Ter | |
| XR_922974.1:n.3293G>A | ||
| XM_006712654.3:c.3158G>A | XP_006712717.1:p.Trp1053Ter | |
| XM_006712655.3:c.1094G>A | XP_006712718.1:p.Trp365Ter | |
| XM_017004569.2:c.3158G>A | XP_016860058.1:p.Trp1053Ter | |
| XM_017004570.2:c.3158G>A | XP_016860059.1:p.Trp1053Ter | |
| XM_017004572.2:c.776G>A | XP_016860061.1:p.Trp259Ter | |
| XM_024453024.1:c.2819G>A | XP_024308792.1:p.Trp940Ter | |
| XM_024453025.1:c.1094G>A | XP_024308793.1:p.Trp365Ter | |
| XR_001738864.2:n.3293G>A | ||
| XR_001738865.2:n.3293G>A | ||
| XR_001738866.2:n.3293G>A | ||
| XR_001738867.2:n.3293G>A | ||
| XR_002959320.1:n.2349G>A | ||
| NM_020919.4:c.3158G>A MANE Select | NP_065970.2:p.Trp1053Ter |