Canonical Allele Identifier: CA868042709
Gene: DAPK1 HGNC NCBI

Linked Data

dbSNP Id: rs1184390650

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.87540581_87540582del , CM000671.2:g.87540581_87540582del GRCh38
NC_000009.11:g.90155496_90155497del , CM000671.1:g.90155496_90155497del GRCh37
NC_000009.10:g.89345316_89345317del NCBI36
NG_029883.1:g.47741_47742del

Transcript Alleles

HGVS Amino-acid Change
ENST00000408954.8:c.62+41442_62+41443del MANE Select ENSP00000386135.3:n.62+41442_62+41443del
ENST00000358077.9:c.62+41442_62+41443del ENSP00000350785.5:n.62+41442_62+41443del
ENST00000408954.7:c.62+41442_62+41443del ENSP00000386135.3:n.62+41442_62+41443del
ENST00000469067.5:n.542+41442_542+41443del
ENST00000469640.6:c.62+41442_62+41443del ENSP00000418885.3:n.62+41442_62+41443del
ENST00000472284.5:c.62+41442_62+41443del ENSP00000417076.1:n.62+41442_62+41443del
ENST00000472344.1:n.196+41442_196+41443del
ENST00000489291.5:c.62+41442_62+41443del ENSP00000417746.1:n.62+41442_62+41443del
ENST00000491893.5:c.62+41442_62+41443del ENSP00000419026.1:n.62+41442_62+41443del
ENST00000496522.5:n.272+41442_272+41443del
ENST00000622514.4:c.62+41442_62+41443del ENSP00000484267.1:n.62+41442_62+41443del
NM_001288729.1:c.62+41442_62+41443del NP_001275658.1:n.62+41442_62+41443del
NM_001288730.1:c.62+41442_62+41443del NP_001275659.1:n.62+41442_62+41443del
NM_001288731.1:c.62+41442_62+41443del NP_001275660.1:n.62+41442_62+41443del
NM_004938.3:c.62+41442_62+41443del NP_004929.2:n.62+41442_62+41443del
XM_005251757.2:c.62+41442_62+41443del XP_005251814.1:n.62+41442_62+41443del
XM_005251757.4:c.62+41442_62+41443del XP_005251814.1:n.62+41442_62+41443del
NM_004938.4:c.62+41442_62+41443del MANE Select NP_004929.2:n.62+41442_62+41443del
NM_001288730.2:c.62+41442_62+41443del NP_001275659.1:n.62+41442_62+41443del
NM_001288731.2:c.62+41442_62+41443del NP_001275660.1:n.62+41442_62+41443del
NM_001288729.2:c.62+41442_62+41443del NP_001275658.1:n.62+41442_62+41443del