Canonical Allele Identifier: CA2500002
Gene: GBE1 HGNC NCBI

Linked Data

dbSNP Id: rs775083576
gnomAD v2: 3-81720086-G-A
gnomAD v3: 3-81670935-G-A
gnomAD v4: 3-81670935-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81670935G>A , CM000665.2:g.81670935G>A GRCh38
NC_000003.11:g.81720086G>A , CM000665.1:g.81720086G>A GRCh37
NC_000003.10:g.81802776G>A NCBI36
NG_011810.1:g.95866C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.332C>T MANE Select ENSP00000410833.2:p.Ser111Leu
ENST00000429644.6:c.332C>T ENSP00000410833.2:p.Ser111Leu
ENST00000477426.1:n.48C>T
ENST00000489715.1:c.209C>T ENSP00000419638.1:p.Ser70Leu
NM_000158.3:c.332C>T NP_000149.3:p.Ser111Leu
NM_000158.4:c.332C>T MANE Select NP_000149.4:p.Ser111Leu