Canonical Allele Identifier: CA196182768

Gene: DAPK1

Linked Data

• dbSNP Id: rs369780808

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.87544165_87544166del , CM000671.2:g.87544165_87544166del	GRCh38
NC_000009.11:g.90159080_90159081del , CM000671.1:g.90159080_90159081del	GRCh37
NC_000009.10:g.89348900_89348901del	NCBI36
NG_029883.1:g.51325_51326del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000408954.8:c.62+45026_62+45027del MANE Select	ENSP00000386135.3:n.62+45026_62+45027del
ENST00000358077.9:c.62+45026_62+45027del	ENSP00000350785.5:n.62+45026_62+45027del
ENST00000408954.7:c.62+45026_62+45027del	ENSP00000386135.3:n.62+45026_62+45027del
ENST00000469067.5:n.542+45026_542+45027del
ENST00000469640.6:c.62+45026_62+45027del	ENSP00000418885.3:n.62+45026_62+45027del
ENST00000472284.5:c.62+45026_62+45027del	ENSP00000417076.1:n.62+45026_62+45027del
ENST00000472344.1:n.196+45026_196+45027del
ENST00000489291.5:c.62+45026_62+45027del	ENSP00000417746.1:n.62+45026_62+45027del
ENST00000491893.5:c.62+45026_62+45027del	ENSP00000419026.1:n.62+45026_62+45027del
ENST00000496522.5:n.272+45026_272+45027del
ENST00000622514.4:c.62+45026_62+45027del	ENSP00000484267.1:n.62+45026_62+45027del
NM_001288729.1:c.62+45026_62+45027del	NP_001275658.1:n.62+45026_62+45027del
NM_001288730.1:c.62+45026_62+45027del	NP_001275659.1:n.62+45026_62+45027del
NM_001288731.1:c.62+45026_62+45027del	NP_001275660.1:n.62+45026_62+45027del
NM_004938.3:c.62+45026_62+45027del	NP_004929.2:n.62+45026_62+45027del
XM_005251757.2:c.62+45026_62+45027del	XP_005251814.1:n.62+45026_62+45027del
XM_005251757.4:c.62+45026_62+45027del	XP_005251814.1:n.62+45026_62+45027del
NM_004938.4:c.62+45026_62+45027del MANE Select	NP_004929.2:n.62+45026_62+45027del
NM_001288730.2:c.62+45026_62+45027del	NP_001275659.1:n.62+45026_62+45027del
NM_001288731.2:c.62+45026_62+45027del	NP_001275660.1:n.62+45026_62+45027del
NM_001288729.2:c.62+45026_62+45027del	NP_001275658.1:n.62+45026_62+45027del