Canonical Allele Identifier: CA1378698106
Gene: GBE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81577905T= , CM000665.2:g.81577905T= GRCh38
NC_000003.11:g.81627056T= , CM000665.1:g.81627056T= GRCh37
NC_000003.10:g.81709746T= NCBI36
NG_011810.1:g.188896A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.1618+20A= MANE Select ENSP00000410833.2:n.1618+20A=
ENST00000429644.6:c.1618+20A= ENSP00000410833.2:n.1618+20A=
ENST00000484687.1:n.19+20A=
ENST00000489715.1:c.1495+20A= ENSP00000419638.1:n.1495+20A=
NM_000158.3:c.1618+20A= NP_000149.3:n.1618+20A=
NM_000158.4:c.1618+20A= MANE Select NP_000149.4:n.1618+20A=