Canonical Allele Identifier: CA375119494
Gene: DOLK HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131708411A>T (hg19) chr9:g.128946132A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128946132A>T , CM000671.2:g.128946132A>T GRCh38
NC_000009.11:g.131708411A>T , CM000671.1:g.131708411A>T GRCh37
NC_000009.10:g.130748232A>T NCBI36
NG_017009.1:g.6602T>A , LRG_744:g.6602T>A
NG_033111.1:g.3440A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.1172T>A MANE Select ENSP00000361667.3:p.Phe391Tyr
ENST00000372586.3:c.1172T>A ENSP00000361667.3:p.Phe391Tyr
ENST00000482796.1:c.39-3057A>T ENSP00000417556.2:n.39-3057A>T
NM_014908.3:c.1172T>A , LRG_744t1:c.1172T>A NP_055723.1:p.Phe391Tyr
NM_014908.4:c.1172T>A MANE Select NP_055723.1:p.Phe391Tyr
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