Canonical Allele Identifier: CA375119093
Gene: DOLK HGNC NCBI

Linked Data

dbSNP Id: rs1361879563
MyVariant Identifiers: chr9:g.131708363G>C (hg19) chr9:g.128946084G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128946084G>C , CM000671.2:g.128946084G>C GRCh38
NC_000009.11:g.131708363G>C , CM000671.1:g.131708363G>C GRCh37
NC_000009.10:g.130748184G>C NCBI36
NG_017009.1:g.6650C>G , LRG_744:g.6650C>G
NG_033111.1:g.3392G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.1220C>G MANE Select ENSP00000361667.3:p.Thr407Arg
ENST00000372586.3:c.1220C>G ENSP00000361667.3:p.Thr407Arg
ENST00000482796.1:c.39-3105G>C ENSP00000417556.2:n.39-3105G>C
NM_014908.3:c.1220C>G , LRG_744t1:c.1220C>G NP_055723.1:p.Thr407Arg
NM_014908.4:c.1220C>G MANE Select NP_055723.1:p.Thr407Arg
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