Canonical Allele Identifier: CA13086839
Gene: DAPK1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3118867

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.87646780A>G , CM000671.2:g.87646780A>G GRCh38
NC_000009.11:g.90261695A>G , CM000671.1:g.90261695A>G GRCh37
NC_000009.10:g.89451515A>G NCBI36
NG_029883.1:g.153940A>G

Transcript Alleles

HGVS Amino-acid change
NM_001288729.1:c.1230+221A>G VV NP_001275658.1:p.=
NM_001288730.1:c.1230+221A>G VV NP_001275659.1:p.=
NM_001288731.1:c.1230+221A>G VV NP_001275660.1:p.=
NM_004938.3:c.1230+221A>G VV NP_004929.2:p.=
XM_005251757.2:c.1230+221A>G XP_005251814.1:p.=
XM_005251757.4:c.1230+221A>G XP_005251814.1:p.=
NM_004938.4:c.1230+221A>G VV MANE Preferred NP_004929.2:p.=
ENST00000358077.9:c.1230+221A>G ENSP00000350785.5:p.=
ENST00000408954.7:c.1230+221A>G ENSP00000386135.3:p.=
ENST00000469067.5:n.1710+221A>G
ENST00000469640.6:c.1230+221A>G ENSP00000418885.3:p.=
ENST00000472284.5:c.1230+221A>G ENSP00000417076.1:p.=
ENST00000489291.5:c.*614+221A>G ENSP00000417746.1:p.=
ENST00000491893.5:c.1230+221A>G ENSP00000419026.1:p.=
ENST00000622514.4:c.1230+221A>G ENSP00000484267.1:p.=