Canonical Allele Identifier: CA1378729098
Gene: GBE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81646399C= , CM000665.2:g.81646399C= GRCh38
NC_000003.11:g.81695550C= , CM000665.1:g.81695550C= GRCh37
NC_000003.10:g.81778240C= NCBI36
NG_011810.1:g.120402G=

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.775G= MANE Select ENSP00000410833.2:p.Ala259=
ENST00000429644.6:c.775G= ENSP00000410833.2:p.Ala259=
ENST00000489715.1:c.652G= ENSP00000419638.1:p.Ala218=
ENST00000498468.1:n.325G=
NM_000158.3:c.775G= NP_000149.3:p.Ala259=
NM_000158.4:c.775G= MANE Select NP_000149.4:p.Ala259=