Canonical Allele Identifier: CA1861954212

Gene: DAPK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.87544332C= , CM000671.2:g.87544332C=	GRCh38
NC_000009.11:g.90159247C= , CM000671.1:g.90159247C=	GRCh37
NC_000009.10:g.89349067C=	NCBI36
NG_029883.1:g.51492C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000408954.8:c.62+45193C= MANE Select	ENSP00000386135.3:n.62+45193C=
ENST00000358077.9:c.62+45193C=	ENSP00000350785.5:n.62+45193C=
ENST00000408954.7:c.62+45193C=	ENSP00000386135.3:n.62+45193C=
ENST00000469067.5:n.542+45193C=
ENST00000469640.6:c.62+45193C=	ENSP00000418885.3:n.62+45193C=
ENST00000472284.5:c.62+45193C=	ENSP00000417076.1:n.62+45193C=
ENST00000472344.1:n.196+45193C=
ENST00000489291.5:c.62+45193C=	ENSP00000417746.1:n.62+45193C=
ENST00000491893.5:c.62+45193C=	ENSP00000419026.1:n.62+45193C=
ENST00000496522.5:n.272+45193C=
ENST00000622514.4:c.62+45193C=	ENSP00000484267.1:n.62+45193C=
NM_001288729.1:c.62+45193C=	NP_001275658.1:n.62+45193C=
NM_001288730.1:c.62+45193C=	NP_001275659.1:n.62+45193C=
NM_001288731.1:c.62+45193C=	NP_001275660.1:n.62+45193C=
NM_004938.3:c.62+45193C=	NP_004929.2:n.62+45193C=
XM_005251757.2:c.62+45193C=	XP_005251814.1:n.62+45193C=
XM_005251757.4:c.62+45193C=	XP_005251814.1:n.62+45193C=
NM_004938.4:c.62+45193C= MANE Select	NP_004929.2:n.62+45193C=
NM_001288730.2:c.62+45193C=	NP_001275659.1:n.62+45193C=
NM_001288731.2:c.62+45193C=	NP_001275660.1:n.62+45193C=
NM_001288729.2:c.62+45193C=	NP_001275658.1:n.62+45193C=