Canonical Allele Identifier: CA2455035119
Gene: GLUD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.121048352C= , CM000685.2:g.121048352C= GRCh38
NC_000023.10:g.120182206C= , CM000685.1:g.120182206C= GRCh37
NC_000023.9:g.120009887C= NCBI36
NG_016456.1:g.5745C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328078.3:c.668C= MANE Select ENSP00000327589.1:p.Ala223=
ENST00000328078.2:c.668C= ENSP00000327589.1:p.Ala223=
NM_012084.3:c.668C= NP_036216.2:p.Ala223=
NM_012084.4:c.668C= MANE Select NP_036216.2:p.Ala223=