Canonical Allele Identifier: CA1378760183
Gene: GBE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81705549A= , CM000665.2:g.81705549A= GRCh38
NC_000003.11:g.81754700A= , CM000665.1:g.81754700A= GRCh37
NC_000003.10:g.81837390A= NCBI36
NG_011810.1:g.61252T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.208T= MANE Select ENSP00000410833.2:p.Ser70=
ENST00000429644.6:c.208T= ENSP00000410833.2:p.Ser70=
ENST00000489715.1:c.85T= ENSP00000419638.1:p.Ser29=
NM_000158.3:c.208T= NP_000149.3:p.Ser70=
NM_000158.4:c.208T= MANE Select NP_000149.4:p.Ser70=