Canonical Allele Identifier: CA2481202741

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238165A= , CM000663.2:g.155238165A=	GRCh38
NC_000001.10:g.155207956A= , CM000663.1:g.155207956A=	GRCh37
NC_000001.9:g.153474580A=	NCBI36
NG_009783.1:g.11533T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368373.8:c.730T= MANE Select	ENSP00000357357.3:p.Tyr244=
ENST00000327247.9:c.730T=	ENSP00000314508.5:p.Tyr244=
ENST00000368373.7:c.730T=	ENSP00000357357.3:p.Tyr244=
ENST00000427500.7:c.583T=	ENSP00000402577.2:p.Tyr195=
ENST00000428024.3:c.469T=	ENSP00000397986.2:p.Tyr157=
ENST00000460156.1:n.517T=
ENST00000484489.5:n.339+1808T=
ENST00000491081.5:n.335T=
ENST00000497670.5:n.353T=
NM_000157.3:c.730T=	NP_000148.2:p.Tyr244=
NM_001005741.2:c.730T=	NP_001005741.1:p.Tyr244=
NM_001005742.2:c.730T=	NP_001005742.1:p.Tyr244=
NM_001171811.1:c.469T=	NP_001165282.1:p.Tyr157=
NM_001171812.1:c.583T=	NP_001165283.1:p.Tyr195=
XM_006711270.1:c.730T=	XP_006711333.1:p.Tyr244=
XM_011509407.1:c.730T=	XP_011507709.1:p.Tyr244=
NM_000157.4:c.730T= MANE Select	NP_000148.2:p.Tyr244=
NM_001005741.3:c.730T=	NP_001005741.1:p.Tyr244=
NM_001005742.3:c.730T=	NP_001005742.1:p.Tyr244=
NM_001171811.2:c.469T=	NP_001165282.1:p.Tyr157=
NM_001171812.2:c.583T=	NP_001165283.1:p.Tyr195=