Canonical Allele Identifier: CA414410232
Gene: GLUD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.120182266C>T (hg19) chrX:g.121048412C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.121048412C>T , CM000685.2:g.121048412C>T GRCh38
NC_000023.10:g.120182266C>T , CM000685.1:g.120182266C>T GRCh37
NC_000023.9:g.120009947C>T NCBI36
NG_016456.1:g.5805C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000328078.3:c.728C>T MANE Select ENSP00000327589.1:p.Thr243Ile
ENST00000328078.2:c.728C>T ENSP00000327589.1:p.Thr243Ile
NM_012084.3:c.728C>T NP_036216.2:p.Thr243Ile
NM_012084.4:c.728C>T MANE Select NP_036216.2:p.Thr243Ile
Search 100 bp 5'
Search 100 bp 3'