Canonical Allele Identifier: CA91138349

Gene: DGKQ

Linked Data

• dbSNP Id: rs189453688
• gnomAD v2: 4-964467-G-T
• gnomAD v3: 4-970679-G-T
• gnomAD v4: 4-970679-G-T
• MyVariant Identifiers: chr4:g.964467G>T (hg19) ; chr4:g.970679G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.970679G>T , CM000666.2:g.970679G>T	GRCh38
NC_000004.11:g.964467G>T , CM000666.1:g.964467G>T	GRCh37
NC_000004.10:g.954467G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273814.8:c.351+314C>A MANE Select	ENSP00000273814.3:n.351+314C>A
ENST00000273814.7:c.351+314C>A	ENSP00000273814.3:n.351+314C>A
ENST00000509465.5:c.191+314C>A
ENST00000510286.1:c.126+314C>A	ENSP00000427268.1:n.126+314C>A
NM_001347.3:c.351+314C>A	NP_001338.2:n.351+314C>A
XM_011513411.1:c.351+314C>A	XP_011511713.1:n.351+314C>A
XM_011513412.1:c.351+314C>A	XP_011511714.1:n.351+314C>A
XM_011513413.1:c.351+314C>A	XP_011511715.1:n.351+314C>A
XM_011513414.1:c.351+314C>A	XP_011511716.1:n.351+314C>A
XM_011513415.1:c.351+314C>A	XP_011511717.1:n.351+314C>A
XM_011513414.2:c.351+314C>A	XP_011511716.1:n.351+314C>A
XM_017007814.1:c.351+314C>A	XP_016863303.1:n.351+314C>A
XM_017007815.1:c.351+314C>A	XP_016863304.1:n.351+314C>A
XR_002959715.1:n.414+314C>A
NM_001347.4:c.351+314C>A MANE Select	NP_001338.2:n.351+314C>A