Canonical Allele Identifier: CA467490785
Gene: DOLK HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131708398A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128946119A>G , CM000671.2:g.128946119A>G GRCh38
NC_000009.11:g.131708398A>G , CM000671.1:g.131708398A>G GRCh37
NC_000009.10:g.130748219A>G NCBI36
NG_017009.1:g.6615T>C , LRG_744:g.6615T>C
NG_033111.1:g.3427A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.1185T>C MANE Select ENSP00000361667.3:p.Phe395=
ENST00000372586.3:c.1185T>C ENSP00000361667.3:p.Phe395=
ENST00000482796.1:c.39-3070A>G ENSP00000417556.2:n.39-3070A>G
NM_014908.3:c.1185T>C , LRG_744t1:c.1185T>C NP_055723.1:p.Phe395=
NM_014908.4:c.1185T>C MANE Select NP_055723.1:p.Phe395=