Canonical Allele Identifier: CA1861970323
Gene: DAPK1 HGNC NCBI

Linked Data

dbSNP Id: rs4878104

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.87578076C>G , CM000671.2:g.87578076C>G GRCh38
NC_000009.11:g.90192991C>G , CM000671.1:g.90192991C>G GRCh37
NC_000009.10:g.89382811C>G NCBI36
NG_029883.1:g.85236C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000408954.8:c.63-26878C>G MANE Select ENSP00000386135.3:n.63-26878C>G
ENST00000358077.9:c.63-26878C>G ENSP00000350785.5:n.63-26878C>G
ENST00000408954.7:c.63-26878C>G ENSP00000386135.3:n.63-26878C>G
ENST00000469067.5:n.543-26878C>G
ENST00000469640.6:c.63-26878C>G ENSP00000418885.3:n.63-26878C>G
ENST00000472284.5:c.63-26878C>G ENSP00000417076.1:n.63-26878C>G
ENST00000472344.1:n.197-26878C>G
ENST00000489291.5:c.63-26878C>G ENSP00000417746.1:n.63-26878C>G
ENST00000491893.5:c.63-26878C>G ENSP00000419026.1:n.63-26878C>G
ENST00000496522.5:n.273-26878C>G
ENST00000622514.4:c.63-26878C>G ENSP00000484267.1:n.63-26878C>G
NM_001288729.1:c.63-26878C>G NP_001275658.1:n.63-26878C>G
NM_001288730.1:c.63-26878C>G NP_001275659.1:n.63-26878C>G
NM_001288731.1:c.63-26878C>G NP_001275660.1:n.63-26878C>G
NM_004938.3:c.63-26878C>G NP_004929.2:n.63-26878C>G
XM_005251757.2:c.63-26878C>G XP_005251814.1:n.63-26878C>G
XM_005251757.4:c.63-26878C>G XP_005251814.1:n.63-26878C>G
NM_004938.4:c.63-26878C>G MANE Select NP_004929.2:n.63-26878C>G
NM_001288730.2:c.63-26878C>G NP_001275659.1:n.63-26878C>G
NM_001288731.2:c.63-26878C>G NP_001275660.1:n.63-26878C>G
NM_001288729.2:c.63-26878C>G NP_001275658.1:n.63-26878C>G