Canonical Allele Identifier: CA1378698116
Gene: GBE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81577925C= , CM000665.2:g.81577925C= GRCh38
NC_000003.11:g.81627076C= , CM000665.1:g.81627076C= GRCh37
NC_000003.10:g.81709766C= NCBI36
NG_011810.1:g.188876G=

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.1618G= MANE Select ENSP00000410833.2:p.Gly540=
ENST00000429644.6:c.1618G= ENSP00000410833.2:p.Gly540=
ENST00000484687.1:n.19G=
ENST00000489715.1:c.1495G= ENSP00000419638.1:p.Gly499=
NM_000158.3:c.1618G= NP_000149.3:p.Gly540=
NM_000158.4:c.1618G= MANE Select NP_000149.4:p.Gly540=