Canonical Allele Identifier: CA1141581086

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155237357G= , CM000663.2:g.155237357G=	GRCh38
NC_000001.10:g.155207148G= , CM000663.1:g.155207148G=	GRCh37
NC_000001.9:g.153473772G=	NCBI36
NG_009783.1:g.12341C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.983C= MANE Select	ENSP00000357357.3:p.Pro328=
ENST00000327247.9:c.983C=	ENSP00000314508.5:p.Pro328=
ENST00000368373.7:c.983C=	ENSP00000357357.3:p.Pro328=
ENST00000427500.7:c.836C=	ENSP00000402577.2:p.Pro279=
ENST00000428024.3:c.722C=	ENSP00000397986.2:p.Pro241=
ENST00000484489.5:n.340-1069C=
ENST00000491081.5:n.588C=
ENST00000497670.5:n.606C=
NM_000157.3:c.983C=	NP_000148.2:p.Pro328=
NM_001005741.2:c.983C=	NP_001005741.1:p.Pro328=
NM_001005742.2:c.983C=	NP_001005742.1:p.Pro328=
NM_001171811.1:c.722C=	NP_001165282.1:p.Pro241=
NM_001171812.1:c.836C=	NP_001165283.1:p.Pro279=
XM_006711270.1:c.983C=	XP_006711333.1:p.Pro328=
XM_011509407.1:c.983C=	XP_011507709.1:p.Pro328=
NM_000157.4:c.983C= MANE Select	NP_000148.2:p.Pro328=
NM_001005741.3:c.983C=	NP_001005741.1:p.Pro328=
NM_001005742.3:c.983C=	NP_001005742.1:p.Pro328=
NM_001171811.2:c.722C=	NP_001165282.1:p.Pro241=
NM_001171812.2:c.836C=	NP_001165283.1:p.Pro279=