Canonical Allele Identifier: CA2455035143
Gene: GLUD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.121048427A= , CM000685.2:g.121048427A= GRCh38
NC_000023.10:g.120182281A= , CM000685.1:g.120182281A= GRCh37
NC_000023.9:g.120009962A= NCBI36
NG_016456.1:g.5820A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328078.3:c.743A= MANE Select ENSP00000327589.1:p.Asp248=
ENST00000328078.2:c.743A= ENSP00000327589.1:p.Asp248=
NM_012084.3:c.743A= NP_036216.2:p.Asp248=
NM_012084.4:c.743A= MANE Select NP_036216.2:p.Asp248=