Canonical Allele Identifier: CA414410261
Gene: GLUD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.120182279T>A (hg19) chrX:g.121048425T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.121048425T>A , CM000685.2:g.121048425T>A GRCh38
NC_000023.10:g.120182279T>A , CM000685.1:g.120182279T>A GRCh37
NC_000023.9:g.120009960T>A NCBI36
NG_016456.1:g.5818T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000328078.3:c.741T>A MANE Select ENSP00000327589.1:p.Tyr247Ter
ENST00000328078.2:c.741T>A ENSP00000327589.1:p.Tyr247Ter
NM_012084.3:c.741T>A NP_036216.2:p.Tyr247Ter
NM_012084.4:c.741T>A MANE Select NP_036216.2:p.Tyr247Ter
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