Canonical Allele Identifier: CA467490123
Gene: DOLK HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131708236C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128945957C>A , CM000671.2:g.128945957C>A GRCh38
NC_000009.11:g.131708236C>A , CM000671.1:g.131708236C>A GRCh37
NC_000009.10:g.130748057C>A NCBI36
NG_017009.1:g.6777G>T , LRG_744:g.6777G>T
NG_033111.1:g.3265C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.1347G>T MANE Select ENSP00000361667.3:p.Val449=
ENST00000372586.3:c.1347G>T ENSP00000361667.3:p.Val449=
ENST00000482796.1:c.39-3232C>A ENSP00000417556.2:n.39-3232C>A
NM_014908.3:c.1347G>T , LRG_744t1:c.1347G>T NP_055723.1:p.Val449=
NM_014908.4:c.1347G>T MANE Select NP_055723.1:p.Val449=
Search 100 bp 5'
Search 100 bp 3'