Canonical Allele Identifier: CA868105566
Gene: DAPK1 HGNC NCBI

Linked Data

dbSNP Id: rs1186126571

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.87620789_87620790insT , CM000671.2:g.87620789_87620790insT GRCh38
NC_000009.11:g.90235704_90235705insT , CM000671.1:g.90235704_90235705insT GRCh37
NC_000009.10:g.89425524_89425525insT NCBI36
NG_029883.1:g.127949_127950insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000408954.8:c.284+15614_284+15615insT MANE Select ENSP00000386135.3:n.284+15614_284+15615insT
ENST00000358077.9:c.284+15614_284+15615insT ENSP00000350785.5:n.284+15614_284+15615insT
ENST00000408954.7:c.284+15614_284+15615insT ENSP00000386135.3:n.284+15614_284+15615insT
ENST00000469067.5:n.764+15614_764+15615insT
ENST00000469640.6:c.284+15614_284+15615insT ENSP00000418885.3:n.284+15614_284+15615insT
ENST00000472284.5:c.284+15614_284+15615insT ENSP00000417076.1:n.284+15614_284+15615insT
ENST00000472344.1:n.418+15614_418+15615insT
ENST00000489291.5:c.284+15614_284+15615insT ENSP00000417746.1:n.284+15614_284+15615insT
ENST00000491893.5:c.284+15614_284+15615insT ENSP00000419026.1:n.284+15614_284+15615insT
ENST00000496522.5:n.494+15614_494+15615insT
ENST00000622514.4:c.284+15614_284+15615insT ENSP00000484267.1:n.284+15614_284+15615insT
NM_001288729.1:c.284+15614_284+15615insT NP_001275658.1:n.284+15614_284+15615insT
NM_001288730.1:c.284+15614_284+15615insT NP_001275659.1:n.284+15614_284+15615insT
NM_001288731.1:c.284+15614_284+15615insT NP_001275660.1:n.284+15614_284+15615insT
NM_004938.3:c.284+15614_284+15615insT NP_004929.2:n.284+15614_284+15615insT
XM_005251757.2:c.284+15614_284+15615insT XP_005251814.1:n.284+15614_284+15615insT
XM_005251757.4:c.284+15614_284+15615insT XP_005251814.1:n.284+15614_284+15615insT
NM_004938.4:c.284+15614_284+15615insT MANE Select NP_004929.2:n.284+15614_284+15615insT
NM_001288730.2:c.284+15614_284+15615insT NP_001275659.1:n.284+15614_284+15615insT
NM_001288731.2:c.284+15614_284+15615insT NP_001275660.1:n.284+15614_284+15615insT
NM_001288729.2:c.284+15614_284+15615insT NP_001275658.1:n.284+15614_284+15615insT