Canonical Allele Identifier: CA467490661
Gene: DOLK HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131708362T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128946083T>G , CM000671.2:g.128946083T>G GRCh38
NC_000009.11:g.131708362T>G , CM000671.1:g.131708362T>G GRCh37
NC_000009.10:g.130748183T>G NCBI36
NG_017009.1:g.6651A>C , LRG_744:g.6651A>C
NG_033111.1:g.3391T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.1221A>C MANE Select ENSP00000361667.3:p.Thr407=
ENST00000372586.3:c.1221A>C ENSP00000361667.3:p.Thr407=
ENST00000482796.1:c.39-3106T>G ENSP00000417556.2:n.39-3106T>G
NM_014908.3:c.1221A>C , LRG_744t1:c.1221A>C NP_055723.1:p.Thr407=
NM_014908.4:c.1221A>C MANE Select NP_055723.1:p.Thr407=
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