Canonical Allele Identifier: CA1378729096
Gene: GBE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81646395G= , CM000665.2:g.81646395G= GRCh38
NC_000003.11:g.81695546G= , CM000665.1:g.81695546G= GRCh37
NC_000003.10:g.81778236G= NCBI36
NG_011810.1:g.120406C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.779C= MANE Select ENSP00000410833.2:p.Ser260=
ENST00000429644.6:c.779C= ENSP00000410833.2:p.Ser260=
ENST00000489715.1:c.656C= ENSP00000419638.1:p.Ser219=
ENST00000498468.1:n.329C=
NM_000158.3:c.779C= NP_000149.3:p.Ser260=
NM_000158.4:c.779C= MANE Select NP_000149.4:p.Ser260=