Canonical Allele Identifier: CA1378729132
Gene: GBE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81646482C= , CM000665.2:g.81646482C= GRCh38
NC_000003.11:g.81695633C= , CM000665.1:g.81695633C= GRCh37
NC_000003.10:g.81778323C= NCBI36
NG_011810.1:g.120319G=

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.692G= MANE Select ENSP00000410833.2:p.Gly231=
ENST00000429644.6:c.692G= ENSP00000410833.2:p.Gly231=
ENST00000489715.1:c.569G= ENSP00000419638.1:p.Gly190=
ENST00000498468.1:n.242G=
NM_000158.3:c.692G= NP_000149.3:p.Gly231=
NM_000158.4:c.692G= MANE Select NP_000149.4:p.Gly231=