Canonical Allele Identifier: CA1335702370
Community Standard Title: NM_152879.3(DGKD):c.156+1528C>A
Gene: DGKD HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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