Linked Data
ClinVar Variation Id:
220581
dbSNP Id:
rs748618094
ExAC:
5:13841167 T / A
gnomAD v2:
5-13841167-T-A
gnomAD v3:
5-13841058-T-A
gnomAD v4:
5-13841058-T-A
COSMIC:
COSM5491880
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13841058T>A , CM000667.2:g.13841058T>A | GRCh38 |
| NC_000005.9:g.13841167T>A , CM000667.1:g.13841167T>A | GRCh37 |
| NC_000005.8:g.13894167T>A | NCBI36 |
| NG_013081.1:g.108423A>T | |
| NG_013081.2:g.108423A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.5557A>T MANE Select | ENSP00000265104.4:p.Lys1853Ter | |
| ENST00000681290.1:c.5512A>T | ENSP00000505288.1:p.Lys1838Ter | |
| ENST00000265104.4:c.5557A>T | ENSP00000265104.4:p.Lys1853Ter | |
| NM_001369.2:c.5557A>T | NP_001360.1:p.Lys1853Ter | |
| XM_005248262.2:c.5512A>T | XP_005248319.1:p.Lys1838Ter | |
| XM_011513990.1:c.5557A>T | XP_011512292.1:p.Lys1853Ter | |
| XR_925598.1:n.5764A>T | ||
| XM_005248262.3:c.5665A>T | XP_005248319.2:p.Lys1889Ter | |
| XM_017009177.1:c.5665A>T | XP_016864666.1:p.Lys1889Ter | |
| XM_017009178.1:c.4570A>T | XP_016864667.1:p.Lys1524Ter | |
| XM_017009179.2:c.4570A>T | XP_016864668.1:p.Lys1524Ter | |
| XM_017009180.1:c.5665A>T | XP_016864669.1:p.Lys1889Ter | |
| XM_017009181.1:c.5665A>T | XP_016864670.1:p.Lys1889Ter | |
| XM_017009182.1:c.5665A>T | XP_016864671.1:p.Lys1889Ter | |
| XM_017009183.1:c.5665A>T | XP_016864672.1:p.Lys1889Ter | |
| XM_017009184.1:c.5665A>T | XP_016864673.1:p.Lys1889Ter | |
| XM_017009185.1:c.754A>T | XP_016864674.1:p.Lys252Ter | |
| XM_017009186.1:c.307A>T | XP_016864675.1:p.Lys103Ter | |
| XM_017009187.1:c.5665A>T | XP_016864676.1:p.Lys1889Ter | |
| XM_024454388.1:c.4570A>T | XP_024310156.1:p.Lys1524Ter | |
| XM_024454389.1:c.4159A>T | XP_024310157.1:p.Lys1387Ter | |
| XR_001742034.1:n.5682A>T | ||
| XR_001742035.1:n.5682A>T | ||
| NM_001369.3:c.5557A>T MANE Select | NP_001360.1:p.Lys1853Ter |