Canonical Allele Identifier: CA353688191
Gene: GBE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81646478G>C , CM000665.2:g.81646478G>C GRCh38
NC_000003.11:g.81695629G>C , CM000665.1:g.81695629G>C GRCh37
NC_000003.10:g.81778319G>C NCBI36
NG_011810.1:g.120323C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.696C>G MANE Select ENSP00000410833.2:p.Tyr232Ter
ENST00000429644.6:c.696C>G ENSP00000410833.2:p.Tyr232Ter
ENST00000489715.1:c.573C>G ENSP00000419638.1:p.Tyr191Ter
ENST00000498468.1:n.246C>G
NM_000158.3:c.696C>G NP_000149.3:p.Tyr232Ter
NM_000158.4:c.696C>G MANE Select NP_000149.4:p.Tyr232Ter