Canonical Allele Identifier: CA15592280
Gene: DAPK1 HGNC NCBI

Linked Data

dbSNP Id: rs4877365

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.87540777G>A , CM000671.2:g.87540777G>A GRCh38
NC_000009.11:g.90155692G>A , CM000671.1:g.90155692G>A GRCh37
NC_000009.10:g.89345512G>A NCBI36
NG_029883.1:g.47937G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000408954.8:c.62+41638G>A MANE Select ENSP00000386135.3:p.=
ENST00000358077.9:c.62+41638G>A ENSP00000350785.5:p.=
ENST00000408954.7:c.62+41638G>A ENSP00000386135.3:p.=
ENST00000469640.6:c.62+41638G>A ENSP00000418885.3:p.=
ENST00000472284.5:c.62+41638G>A ENSP00000417076.1:p.=
ENST00000489291.5:c.62+41638G>A ENSP00000417746.1:p.=
ENST00000491893.5:c.62+41638G>A ENSP00000419026.1:p.=
ENST00000622514.4:c.62+41638G>A ENSP00000484267.1:p.=
NM_001288729.1:c.62+41638G>A NP_001275658.1:p.=
NM_001288730.1:c.62+41638G>A NP_001275659.1:p.=
NM_001288731.1:c.62+41638G>A NP_001275660.1:p.=
NM_004938.3:c.62+41638G>A NP_004929.2:p.=
XM_005251757.2:c.62+41638G>A XP_005251814.1:p.=
XM_005251757.4:c.62+41638G>A XP_005251814.1:p.=
NM_004938.4:c.62+41638G>A MANE Select NP_004929.2:p.=
NM_001288730.2:c.62+41638G>A NP_001275659.1:p.=
NM_001288731.2:c.62+41638G>A NP_001275660.1:p.=
NM_001288729.2:c.62+41638G>A NP_001275658.1:p.=