Canonical Allele Identifier: CA467490863
Gene: DOLK HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131708422A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128946143A>T , CM000671.2:g.128946143A>T GRCh38
NC_000009.11:g.131708422A>T , CM000671.1:g.131708422A>T GRCh37
NC_000009.10:g.130748243A>T NCBI36
NG_017009.1:g.6591T>A , LRG_744:g.6591T>A
NG_033111.1:g.3451A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.1161T>A MANE Select ENSP00000361667.3:p.Thr387=
ENST00000372586.3:c.1161T>A ENSP00000361667.3:p.Thr387=
ENST00000482796.1:c.39-3046A>T ENSP00000417556.2:n.39-3046A>T
NM_014908.3:c.1161T>A , LRG_744t1:c.1161T>A NP_055723.1:p.Thr387=
NM_014908.4:c.1161T>A MANE Select NP_055723.1:p.Thr387=