Canonical Allele Identifier: CA353688229
Gene: GBE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81648864T>G , CM000665.2:g.81648864T>G GRCh38
NC_000003.11:g.81698015T>G , CM000665.1:g.81698015T>G GRCh37
NC_000003.10:g.81780705T>G NCBI36
NG_011810.1:g.117937A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.683A>C MANE Select ENSP00000410833.2:p.Lys228Thr
ENST00000429644.6:c.683A>C ENSP00000410833.2:p.Lys228Thr
ENST00000489715.1:c.560A>C ENSP00000419638.1:p.Lys187Thr
ENST00000498468.1:n.211A>C
NM_000158.3:c.683A>C NP_000149.3:p.Lys228Thr
NM_000158.4:c.683A>C MANE Select NP_000149.4:p.Lys228Thr