Canonical Allele Identifier: CA2481201961

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155236349T= , CM000663.2:g.155236349T=	GRCh38
NC_000001.10:g.155206140T= , CM000663.1:g.155206140T=	GRCh37
NC_000001.9:g.153472764T=	NCBI36
NG_009783.1:g.13349A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.1120A= MANE Select	ENSP00000357357.3:p.Met374=
ENST00000327247.9:c.1120A=	ENSP00000314508.5:p.Met374=
ENST00000368373.7:c.1120A=	ENSP00000357357.3:p.Met374=
ENST00000427500.7:c.973A=	ENSP00000402577.2:p.Met325=
ENST00000428024.3:c.859A=	ENSP00000397986.2:p.Met287=
ENST00000478472.1:n.111A=
ENST00000484489.5:n.340-61A=
ENST00000491081.5:n.725A=
NM_000157.3:c.1120A=	NP_000148.2:p.Met374=
NM_001005741.2:c.1120A=	NP_001005741.1:p.Met374=
NM_001005742.2:c.1120A=	NP_001005742.1:p.Met374=
NM_001171811.1:c.859A=	NP_001165282.1:p.Met287=
NM_001171812.1:c.973A=	NP_001165283.1:p.Met325=
XM_006711270.1:c.1120A=	XP_006711333.1:p.Met374=
XM_011509407.1:c.1120A=	XP_011507709.1:p.Met374=
NM_000157.4:c.1120A= MANE Select	NP_000148.2:p.Met374=
NM_001005741.3:c.1120A=	NP_001005741.1:p.Met374=
NM_001005742.3:c.1120A=	NP_001005742.1:p.Met374=
NM_001171811.2:c.859A=	NP_001165282.1:p.Met287=
NM_001171812.2:c.973A=	NP_001165283.1:p.Met325=