Canonical Allele Identifier: CA588709723
Gene: DAPK1 HGNC NCBI

Linked Data

dbSNP Id: rs990853426

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.87620790del , CM000671.2:g.87620790del GRCh38
NC_000009.11:g.90235705del , CM000671.1:g.90235705del GRCh37
NC_000009.10:g.89425525del NCBI36
NG_029883.1:g.127950del

Transcript Alleles

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