Canonical Allele Identifier: CA549144569

Gene: DGKQ

Linked Data

• dbSNP Id: rs1278225665
• gnomAD v2: 4-964750-T-C
• gnomAD v4: 4-970962-T-C
• MyVariant Identifiers: chr4:g.964750T>C (hg19) ; chr4:g.970962T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.970962T>C , CM000666.2:g.970962T>C	GRCh38
NC_000004.11:g.964750T>C , CM000666.1:g.964750T>C	GRCh37
NC_000004.10:g.954750T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273814.8:c.351+31A>G MANE Select	ENSP00000273814.3:n.351+31A>G
ENST00000273814.7:c.351+31A>G	ENSP00000273814.3:n.351+31A>G
ENST00000509465.5:c.191+31A>G
ENST00000510286.1:c.126+31A>G	ENSP00000427268.1:n.126+31A>G
NM_001347.3:c.351+31A>G	NP_001338.2:n.351+31A>G
XM_011513411.1:c.351+31A>G	XP_011511713.1:n.351+31A>G
XM_011513412.1:c.351+31A>G	XP_011511714.1:n.351+31A>G
XM_011513413.1:c.351+31A>G	XP_011511715.1:n.351+31A>G
XM_011513414.1:c.351+31A>G	XP_011511716.1:n.351+31A>G
XM_011513415.1:c.351+31A>G	XP_011511717.1:n.351+31A>G
XM_011513414.2:c.351+31A>G	XP_011511716.1:n.351+31A>G
XM_017007814.1:c.351+31A>G	XP_016863303.1:n.351+31A>G
XM_017007815.1:c.351+31A>G	XP_016863304.1:n.351+31A>G
XR_002959715.1:n.414+31A>G
NM_001347.4:c.351+31A>G MANE Select	NP_001338.2:n.351+31A>G