Canonical Allele Identifier: CA1861977400

Gene: DAPK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.87594165_87594174delinsGTTGTTTGTT , CM000671.2:g.87594165_87594174delinsGTTGTTTGTT	GRCh38
NC_000009.11:g.90209080_90209089delinsGTTGTTTGTT , CM000671.1:g.90209080_90209089delinsGTTGTTTGTT	GRCh37
NC_000009.10:g.89398900_89398909delinsGTTGTTTGTT	NCBI36
NG_029883.1:g.101325_101334delinsGTTGTTTGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000408954.8:c.63-10789_63-10780delinsGTTGTTTGTT MANE Select	ENSP00000386135.3:n.63-10789_63-10780delinsGTTGTTTGTT
ENST00000358077.9:c.63-10789_63-10780delinsGTTGTTTGTT	ENSP00000350785.5:n.63-10789_63-10780delinsGTTGTTTGTT
ENST00000408954.7:c.63-10789_63-10780delinsGTTGTTTGTT	ENSP00000386135.3:n.63-10789_63-10780delinsGTTGTTTGTT
ENST00000469067.5:n.543-10789_543-10780delinsGTTGTTTGTT
ENST00000469640.6:c.63-10789_63-10780delinsGTTGTTTGTT	ENSP00000418885.3:n.63-10789_63-10780delinsGTTGTTTGTT
ENST00000472284.5:c.63-10789_63-10780delinsGTTGTTTGTT	ENSP00000417076.1:n.63-10789_63-10780delinsGTTGTTTGTT
ENST00000472344.1:n.197-10789_197-10780delinsGTTGTTTGTT
ENST00000489291.5:c.63-10789_63-10780delinsGTTGTTTGTT	ENSP00000417746.1:n.63-10789_63-10780delinsGTTGTTTGTT
ENST00000491893.5:c.63-10789_63-10780delinsGTTGTTTGTT	ENSP00000419026.1:n.63-10789_63-10780delinsGTTGTTTGTT
ENST00000496522.5:n.273-10789_273-10780delinsGTTGTTTGTT
ENST00000622514.4:c.63-10789_63-10780delinsGTTGTTTGTT	ENSP00000484267.1:n.63-10789_63-10780delinsGTTGTTTGTT
NM_001288729.1:c.63-10789_63-10780delinsGTTGTTTGTT	NP_001275658.1:n.63-10789_63-10780delinsGTTGTTTGTT
NM_001288730.1:c.63-10789_63-10780delinsGTTGTTTGTT	NP_001275659.1:n.63-10789_63-10780delinsGTTGTTTGTT
NM_001288731.1:c.63-10789_63-10780delinsGTTGTTTGTT	NP_001275660.1:n.63-10789_63-10780delinsGTTGTTTGTT
NM_004938.3:c.63-10789_63-10780delinsGTTGTTTGTT	NP_004929.2:n.63-10789_63-10780delinsGTTGTTTGTT
XM_005251757.2:c.63-10789_63-10780delinsGTTGTTTGTT	XP_005251814.1:n.63-10789_63-10780delinsGTTGTTTGTT
XM_005251757.4:c.63-10789_63-10780delinsGTTGTTTGTT	XP_005251814.1:n.63-10789_63-10780delinsGTTGTTTGTT
NM_004938.4:c.63-10789_63-10780delinsGTTGTTTGTT MANE Select	NP_004929.2:n.63-10789_63-10780delinsGTTGTTTGTT
NM_001288730.2:c.63-10789_63-10780delinsGTTGTTTGTT	NP_001275659.1:n.63-10789_63-10780delinsGTTGTTTGTT
NM_001288731.2:c.63-10789_63-10780delinsGTTGTTTGTT	NP_001275660.1:n.63-10789_63-10780delinsGTTGTTTGTT
NM_001288729.2:c.63-10789_63-10780delinsGTTGTTTGTT	NP_001275658.1:n.63-10789_63-10780delinsGTTGTTTGTT