Canonical Allele Identifier: CA353684745
Gene: GBE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.81627167A>T (hg19) chr3:g.81578016A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81578016A>T , CM000665.2:g.81578016A>T GRCh38
NC_000003.11:g.81627167A>T , CM000665.1:g.81627167A>T GRCh37
NC_000003.10:g.81709857A>T NCBI36
NG_011810.1:g.188785T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.1527T>A MANE Select ENSP00000410833.2:p.Phe509Leu
ENST00000429644.6:c.1527T>A ENSP00000410833.2:p.Phe509Leu
ENST00000489715.1:c.1404T>A ENSP00000419638.1:p.Phe468Leu
NM_000158.3:c.1527T>A NP_000149.3:p.Phe509Leu
NM_000158.4:c.1527T>A MANE Select NP_000149.4:p.Phe509Leu
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