Canonical Allele Identifier: CA467490739
Gene: DOLK HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131708386T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128946107T>A , CM000671.2:g.128946107T>A GRCh38
NC_000009.11:g.131708386T>A , CM000671.1:g.131708386T>A GRCh37
NC_000009.10:g.130748207T>A NCBI36
NG_017009.1:g.6627A>T , LRG_744:g.6627A>T
NG_033111.1:g.3415T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.1197A>T MANE Select ENSP00000361667.3:p.Arg399=
ENST00000372586.3:c.1197A>T ENSP00000361667.3:p.Arg399=
ENST00000482796.1:c.39-3082T>A ENSP00000417556.2:n.39-3082T>A
NM_014908.3:c.1197A>T , LRG_744t1:c.1197A>T NP_055723.1:p.Arg399=
NM_014908.4:c.1197A>T MANE Select NP_055723.1:p.Arg399=