Canonical Allele Identifier: CA1378729127
Gene: GBE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81646473C= , CM000665.2:g.81646473C= GRCh38
NC_000003.11:g.81695624C= , CM000665.1:g.81695624C= GRCh37
NC_000003.10:g.81778314C= NCBI36
NG_011810.1:g.120328G=

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.701G= MANE Select ENSP00000410833.2:p.Cys234=
ENST00000429644.6:c.701G= ENSP00000410833.2:p.Cys234=
ENST00000489715.1:c.578G= ENSP00000419638.1:p.Cys193=
ENST00000498468.1:n.251G=
NM_000158.3:c.701G= NP_000149.3:p.Cys234=
NM_000158.4:c.701G= MANE Select NP_000149.4:p.Cys234=