Canonical Allele Identifier: CA1378698158
Gene: GBE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81578022A= , CM000665.2:g.81578022A= GRCh38
NC_000003.11:g.81627173A= , CM000665.1:g.81627173A= GRCh37
NC_000003.10:g.81709863A= NCBI36
NG_011810.1:g.188779T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.1521T= MANE Select ENSP00000410833.2:p.Thr507=
ENST00000429644.6:c.1521T= ENSP00000410833.2:p.Thr507=
ENST00000489715.1:c.1398T= ENSP00000419638.1:p.Thr466=
NM_000158.3:c.1521T= NP_000149.3:p.Thr507=
NM_000158.4:c.1521T= MANE Select NP_000149.4:p.Thr507=