Canonical Allele Identifier: CA2599504271
Gene: DAPK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.87540382_87540383insAGG , CM000671.2:g.87540382_87540383insAGG GRCh38
NC_000009.11:g.90155297_90155298insAGG , CM000671.1:g.90155297_90155298insAGG GRCh37
NC_000009.10:g.89345117_89345118insAGG NCBI36
NG_029883.1:g.47542_47543insAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000408954.8:c.62+41243_62+41244insAGG MANE Select ENSP00000386135.3:n.62+41243_62+41244insAGG
ENST00000358077.9:c.62+41243_62+41244insAGG ENSP00000350785.5:n.62+41243_62+41244insAGG
ENST00000408954.7:c.62+41243_62+41244insAGG ENSP00000386135.3:n.62+41243_62+41244insAGG
ENST00000469067.5:n.542+41243_542+41244insAGG
ENST00000469640.6:c.62+41243_62+41244insAGG ENSP00000418885.3:n.62+41243_62+41244insAGG
ENST00000472284.5:c.62+41243_62+41244insAGG ENSP00000417076.1:n.62+41243_62+41244insAGG
ENST00000472344.1:n.196+41243_196+41244insAGG
ENST00000489291.5:c.62+41243_62+41244insAGG ENSP00000417746.1:n.62+41243_62+41244insAGG
ENST00000491893.5:c.62+41243_62+41244insAGG ENSP00000419026.1:n.62+41243_62+41244insAGG
ENST00000496522.5:n.272+41243_272+41244insAGG
ENST00000622514.4:c.62+41243_62+41244insAGG ENSP00000484267.1:n.62+41243_62+41244insAGG
NM_001288729.1:c.62+41243_62+41244insAGG NP_001275658.1:n.62+41243_62+41244insAGG
NM_001288730.1:c.62+41243_62+41244insAGG NP_001275659.1:n.62+41243_62+41244insAGG
NM_001288731.1:c.62+41243_62+41244insAGG NP_001275660.1:n.62+41243_62+41244insAGG
NM_004938.3:c.62+41243_62+41244insAGG NP_004929.2:n.62+41243_62+41244insAGG
XM_005251757.2:c.62+41243_62+41244insAGG XP_005251814.1:n.62+41243_62+41244insAGG
XM_005251757.4:c.62+41243_62+41244insAGG XP_005251814.1:n.62+41243_62+41244insAGG
NM_004938.4:c.62+41243_62+41244insAGG MANE Select NP_004929.2:n.62+41243_62+41244insAGG
NM_001288730.2:c.62+41243_62+41244insAGG NP_001275659.1:n.62+41243_62+41244insAGG
NM_001288731.2:c.62+41243_62+41244insAGG NP_001275660.1:n.62+41243_62+41244insAGG
NM_001288729.2:c.62+41243_62+41244insAGG NP_001275658.1:n.62+41243_62+41244insAGG