Canonical Allele Identifier: CA1142176971

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238631G= , CM000663.2:g.155238631G=	GRCh38
NC_000001.10:g.155208422G= , CM000663.1:g.155208422G=	GRCh37
NC_000001.9:g.153475046G=	NCBI36
NG_009783.1:g.11067C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368373.8:c.474C= MANE Select	ENSP00000357357.3:p.Ile158=
ENST00000327247.9:c.474C=	ENSP00000314508.5:p.Ile158=
ENST00000368373.7:c.474C=	ENSP00000357357.3:p.Ile158=
ENST00000427500.7:c.327C=	ENSP00000402577.2:p.Ile109=
ENST00000428024.3:c.213C=	ENSP00000397986.2:p.Ile71=
ENST00000460156.1:n.261C=
ENST00000473570.5:n.795C=
ENST00000484489.5:n.339+1342C=
ENST00000491081.5:n.79C=
ENST00000493842.5:n.812C=
ENST00000497670.5:n.97C=
NM_000157.3:c.474C=	NP_000148.2:p.Ile158=
NM_001005741.2:c.474C=	NP_001005741.1:p.Ile158=
NM_001005742.2:c.474C=	NP_001005742.1:p.Ile158=
NM_001171811.1:c.213C=	NP_001165282.1:p.Ile71=
NM_001171812.1:c.327C=	NP_001165283.1:p.Ile109=
XM_006711270.1:c.474C=	XP_006711333.1:p.Ile158=
XM_011509407.1:c.474C=	XP_011507709.1:p.Ile158=
NM_000157.4:c.474C= MANE Select	NP_000148.2:p.Ile158=
NM_001005741.3:c.474C=	NP_001005741.1:p.Ile158=
NM_001005742.3:c.474C=	NP_001005742.1:p.Ile158=
NM_001171811.2:c.213C=	NP_001165282.1:p.Ile71=
NM_001171812.2:c.327C=	NP_001165283.1:p.Ile109=