Canonical Allele Identifier: CA195548357
Gene: DAPK1 HGNC NCBI

Linked Data

dbSNP Id: rs373542999

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.87620703_87620708del , CM000671.2:g.87620703_87620708del GRCh38
NC_000009.11:g.90235618_90235623del , CM000671.1:g.90235618_90235623del GRCh37
NC_000009.10:g.89425438_89425443del NCBI36
NG_029883.1:g.127863_127868del

Transcript Alleles

HGVS Amino-acid Change
ENST00000408954.8:c.284+15528_284+15533del MANE Select ENSP00000386135.3:n.284+15528_284+15533del
ENST00000358077.9:c.284+15528_284+15533del ENSP00000350785.5:n.284+15528_284+15533del
ENST00000408954.7:c.284+15528_284+15533del ENSP00000386135.3:n.284+15528_284+15533del
ENST00000469067.5:n.764+15528_764+15533del
ENST00000469640.6:c.284+15528_284+15533del ENSP00000418885.3:n.284+15528_284+15533del
ENST00000472284.5:c.284+15528_284+15533del ENSP00000417076.1:n.284+15528_284+15533del
ENST00000472344.1:n.418+15528_418+15533del
ENST00000489291.5:c.284+15528_284+15533del ENSP00000417746.1:n.284+15528_284+15533del
ENST00000491893.5:c.284+15528_284+15533del ENSP00000419026.1:n.284+15528_284+15533del
ENST00000496522.5:n.494+15528_494+15533del
ENST00000622514.4:c.284+15528_284+15533del ENSP00000484267.1:n.284+15528_284+15533del
NM_001288729.1:c.284+15528_284+15533del NP_001275658.1:n.284+15528_284+15533del
NM_001288730.1:c.284+15528_284+15533del NP_001275659.1:n.284+15528_284+15533del
NM_001288731.1:c.284+15528_284+15533del NP_001275660.1:n.284+15528_284+15533del
NM_004938.3:c.284+15528_284+15533del NP_004929.2:n.284+15528_284+15533del
XM_005251757.2:c.284+15528_284+15533del XP_005251814.1:n.284+15528_284+15533del
XM_005251757.4:c.284+15528_284+15533del XP_005251814.1:n.284+15528_284+15533del
NM_004938.4:c.284+15528_284+15533del MANE Select NP_004929.2:n.284+15528_284+15533del
NM_001288730.2:c.284+15528_284+15533del NP_001275659.1:n.284+15528_284+15533del
NM_001288731.2:c.284+15528_284+15533del NP_001275660.1:n.284+15528_284+15533del
NM_001288729.2:c.284+15528_284+15533del NP_001275658.1:n.284+15528_284+15533del