Canonical Allele Identifier: CA11102004
Community Standard Title: NM_152879.3(DGKD):c.156+1528C>G
Gene: DGKD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233356202C>G , CM000664.2:g.233356202C>G GRCh38
NC_000002.11:g.234264848C>G , CM000664.1:g.234264848C>G GRCh37
NC_000002.10:g.233929587C>G NCBI36
NG_029495.1:g.6696C>G

Transcript Alleles

HGVS Amino-acid Change
NM_152879.3:c.156+1528C>G MANE Select NP_690618.2:n.156+1528C>G
ENST00000264057.7:c.156+1528C>G MANE Select ENSP00000264057.2:n.156+1528C>G
NM_152879.2:c.156+1528C>G NP_690618.2:n.156+1528C>G
ENST00000264057.6:c.156+1528C>G ENSP00000264057.2:n.156+1528C>G
ENST00000427930.5:c.156+1528C>G ENSP00000407938.1:n.156+1528C>G
ENST00000442524.4:c.103+1528C>G
XM_011512028.3:c.-894C>G XP_011510330.1:n.-894C>G
XM_011512029.3:c.-894C>G XP_011510331.1:n.-894C>G
XM_011512033.3:c.-894C>G XP_011510335.1:n.-894C>G
XM_011512036.1:c.36+543C>G XP_011510338.1:n.36+543C>G
XM_011512039.2:c.-894C>G XP_011510341.1:n.-894C>G
XM_017005138.2:c.36+543C>G XP_016860627.1:n.36+543C>G
XR_923050.2:n.512C>G