Canonical Allele Identifier: CA91138326
Gene: DGKQ HGNC NCBI

Linked Data

dbSNP Id: rs370378827
gnomAD v2: 4-964423-C-T
gnomAD v3: 4-970635-C-T
gnomAD v4: 4-970635-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.970635C>T , CM000666.2:g.970635C>T GRCh38
NC_000004.11:g.964423C>T , CM000666.1:g.964423C>T GRCh37
NC_000004.10:g.954423C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000273814.8:c.351+358G>A MANE Select ENSP00000273814.3:n.351+358G>A
ENST00000273814.7:c.351+358G>A ENSP00000273814.3:n.351+358G>A
ENST00000509465.5:c.191+358G>A
ENST00000510286.1:c.126+358G>A ENSP00000427268.1:n.126+358G>A
NM_001347.3:c.351+358G>A NP_001338.2:n.351+358G>A
XM_011513411.1:c.351+358G>A XP_011511713.1:n.351+358G>A
XM_011513412.1:c.351+358G>A XP_011511714.1:n.351+358G>A
XM_011513413.1:c.351+358G>A XP_011511715.1:n.351+358G>A
XM_011513414.1:c.351+358G>A XP_011511716.1:n.351+358G>A
XM_011513415.1:c.351+358G>A XP_011511717.1:n.351+358G>A
XM_011513414.2:c.351+358G>A XP_011511716.1:n.351+358G>A
XM_017007814.1:c.351+358G>A XP_016863303.1:n.351+358G>A
XM_017007815.1:c.351+358G>A XP_016863304.1:n.351+358G>A
XR_002959715.1:n.414+358G>A
NM_001347.4:c.351+358G>A MANE Select NP_001338.2:n.351+358G>A