Canonical Allele Identifier: CA467490861
Gene: DOLK HGNC NCBI

Linked Data

gnomAD v4: 9-128946143-A-C
MyVariant Identifiers: chr9:g.131708422A>C (hg19)
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Genomic Alleles

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

Transcript Alleles

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