Canonical Allele Identifier: CA1141104629

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155239932C= , CM000663.2:g.155239932C=	GRCh38
NC_000001.10:g.155209723C= , CM000663.1:g.155209723C=	GRCh37
NC_000001.9:g.153476347C=	NCBI36
NG_009783.1:g.9766G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.261G= MANE Select	ENSP00000357357.3:p.Arg87=
ENST00000327247.9:c.261G=	ENSP00000314508.5:p.Arg87=
ENST00000368373.7:c.261G=	ENSP00000357357.3:p.Arg87=
ENST00000427500.7:c.261G=	ENSP00000402577.2:p.Arg87=
ENST00000428024.3:c.-1G=	ENSP00000397986.2:n.-1G=
ENST00000467918.5:n.451G=
ENST00000473570.5:n.582G=
ENST00000484489.5:n.339+41G=
ENST00000493842.5:n.599G=
ENST00000497670.5:n.31G=
NM_000157.3:c.261G=	NP_000148.2:p.Arg87=
NM_001005741.2:c.261G=	NP_001005741.1:p.Arg87=
NM_001005742.2:c.261G=	NP_001005742.1:p.Arg87=
NM_001171811.1:c.-1G=	NP_001165282.1:n.-1G=
NM_001171812.1:c.261G=	NP_001165283.1:p.Arg87=
XM_006711270.1:c.261G=	XP_006711333.1:p.Arg87=
XM_011509407.1:c.261G=	XP_011507709.1:p.Arg87=
NM_000157.4:c.261G= MANE Select	NP_000148.2:p.Arg87=
NM_001005741.3:c.261G=	NP_001005741.1:p.Arg87=
NM_001005742.3:c.261G=	NP_001005742.1:p.Arg87=
NM_001171811.2:c.-1G=	NP_001165282.1:n.-1G=
NM_001171812.2:c.261G=	NP_001165283.1:p.Arg87=