Canonical Allele Identifier: CA1378729106
Gene: GBE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81646421G= , CM000665.2:g.81646421G= GRCh38
NC_000003.11:g.81695572G= , CM000665.1:g.81695572G= GRCh37
NC_000003.10:g.81778262G= NCBI36
NG_011810.1:g.120380C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.753C= MANE Select ENSP00000410833.2:p.Tyr251=
ENST00000429644.6:c.753C= ENSP00000410833.2:p.Tyr251=
ENST00000489715.1:c.630C= ENSP00000419638.1:p.Tyr210=
ENST00000498468.1:n.303C=
NM_000158.3:c.753C= NP_000149.3:p.Tyr251=
NM_000158.4:c.753C= MANE Select NP_000149.4:p.Tyr251=