Canonical Allele Identifier: CA467490037
Gene: DOLK HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131707984C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128945705C>G , CM000671.2:g.128945705C>G GRCh38
NC_000009.11:g.131707984C>G , CM000671.1:g.131707984C>G GRCh37
NC_000009.10:g.130747805C>G NCBI36
NG_017009.1:g.7029G>C , LRG_744:g.7029G>C
NG_033111.1:g.3013C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.1599G>C MANE Select ENSP00000361667.3:p.Leu533=
ENST00000372586.3:c.1599G>C ENSP00000361667.3:p.Leu533=
ENST00000482796.1:c.39-3484C>G ENSP00000417556.2:n.39-3484C>G
NM_014908.3:c.1599G>C , LRG_744t1:c.1599G>C NP_055723.1:p.Leu533=
NM_014908.4:c.1599G>C MANE Select NP_055723.1:p.Leu533=
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