Canonical Allele Identifier: CA414410213
Gene: GLUD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.120182258T>A (hg19) chrX:g.121048404T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.121048404T>A , CM000685.2:g.121048404T>A GRCh38
NC_000023.10:g.120182258T>A , CM000685.1:g.120182258T>A GRCh37
NC_000023.9:g.120009939T>A NCBI36
NG_016456.1:g.5797T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000328078.3:c.720T>A MANE Select ENSP00000327589.1:p.Tyr240Ter
ENST00000328078.2:c.720T>A ENSP00000327589.1:p.Tyr240Ter
NM_012084.3:c.720T>A NP_036216.2:p.Tyr240Ter
NM_012084.4:c.720T>A MANE Select NP_036216.2:p.Tyr240Ter
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