Canonical Allele Identifier: CA195548427

Gene: DAPK1

Linked Data

• dbSNP Id: rs1019231547
• gnomAD v3: 9-87620847-G-C
• gnomAD v4: 9-87620847-G-C
• MyVariant Identifiers: chr9:g.90235762G>C (hg19) ; chr9:g.87620847G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.87620847G>C , CM000671.2:g.87620847G>C	GRCh38
NC_000009.11:g.90235762G>C , CM000671.1:g.90235762G>C	GRCh37
NC_000009.10:g.89425582G>C	NCBI36
NG_029883.1:g.128007G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000408954.8:c.284+15672G>C MANE Select	ENSP00000386135.3:n.284+15672G>C
ENST00000358077.9:c.284+15672G>C	ENSP00000350785.5:n.284+15672G>C
ENST00000408954.7:c.284+15672G>C	ENSP00000386135.3:n.284+15672G>C
ENST00000469067.5:n.764+15672G>C
ENST00000469640.6:c.284+15672G>C	ENSP00000418885.3:n.284+15672G>C
ENST00000472284.5:c.284+15672G>C	ENSP00000417076.1:n.284+15672G>C
ENST00000472344.1:n.418+15672G>C
ENST00000489291.5:c.284+15672G>C	ENSP00000417746.1:n.284+15672G>C
ENST00000491893.5:c.284+15672G>C	ENSP00000419026.1:n.284+15672G>C
ENST00000496522.5:n.494+15672G>C
ENST00000622514.4:c.284+15672G>C	ENSP00000484267.1:n.284+15672G>C
NM_001288729.1:c.284+15672G>C	NP_001275658.1:n.284+15672G>C
NM_001288730.1:c.284+15672G>C	NP_001275659.1:n.284+15672G>C
NM_001288731.1:c.284+15672G>C	NP_001275660.1:n.284+15672G>C
NM_004938.3:c.284+15672G>C	NP_004929.2:n.284+15672G>C
XM_005251757.2:c.284+15672G>C	XP_005251814.1:n.284+15672G>C
XM_005251757.4:c.284+15672G>C	XP_005251814.1:n.284+15672G>C
NM_004938.4:c.284+15672G>C MANE Select	NP_004929.2:n.284+15672G>C
NM_001288730.2:c.284+15672G>C	NP_001275659.1:n.284+15672G>C
NM_001288731.2:c.284+15672G>C	NP_001275660.1:n.284+15672G>C
NM_001288729.2:c.284+15672G>C	NP_001275658.1:n.284+15672G>C