Canonical Allele Identifier: CA355941653

Gene: DGKQ

Linked Data

• dbSNP Id: rs1311644048
• gnomAD v2: 4-964814-G-C
• gnomAD v4: 4-971026-G-C
• MyVariant Identifiers: chr4:g.964814G>C (hg19) ; chr4:g.971026G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.971026G>C , CM000666.2:g.971026G>C	GRCh38
NC_000004.11:g.964814G>C , CM000666.1:g.964814G>C	GRCh37
NC_000004.10:g.954814G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273814.8:c.318C>G MANE Select	ENSP00000273814.3:p.Ile106Met
ENST00000273814.7:c.318C>G	ENSP00000273814.3:p.Ile106Met
ENST00000509465.5:c.158C>G
ENST00000510286.1:c.93C>G	ENSP00000427268.1:p.Ile31Met
NM_001347.3:c.318C>G	NP_001338.2:p.Ile106Met
XM_011513411.1:c.318C>G	XP_011511713.1:p.Ile106Met
XM_011513412.1:c.318C>G	XP_011511714.1:p.Ile106Met
XM_011513413.1:c.318C>G	XP_011511715.1:p.Ile106Met
XM_011513414.1:c.318C>G	XP_011511716.1:p.Ile106Met
XM_011513415.1:c.318C>G	XP_011511717.1:p.Ile106Met
XM_011513414.2:c.318C>G	XP_011511716.1:p.Ile106Met
XM_017007814.1:c.318C>G	XP_016863303.1:p.Ile106Met
XM_017007815.1:c.318C>G	XP_016863304.1:p.Ile106Met
XR_002959715.1:n.381C>G
NM_001347.4:c.318C>G MANE Select	NP_001338.2:p.Ile106Met