Canonical Allele Identifier: CA1140972415

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238164T= , CM000663.2:g.155238164T=	GRCh38
NC_000001.10:g.155207955T= , CM000663.1:g.155207955T=	GRCh37
NC_000001.9:g.153474579T=	NCBI36
NG_009783.1:g.11534A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.731A= MANE Select	ENSP00000357357.3:p.Tyr244=
ENST00000327247.9:c.731A=	ENSP00000314508.5:p.Tyr244=
ENST00000368373.7:c.731A=	ENSP00000357357.3:p.Tyr244=
ENST00000427500.7:c.584A=	ENSP00000402577.2:p.Tyr195=
ENST00000428024.3:c.470A=	ENSP00000397986.2:p.Tyr157=
ENST00000460156.1:n.518A=
ENST00000484489.5:n.339+1809A=
ENST00000491081.5:n.336A=
ENST00000497670.5:n.354A=
NM_000157.3:c.731A=	NP_000148.2:p.Tyr244=
NM_001005741.2:c.731A=	NP_001005741.1:p.Tyr244=
NM_001005742.2:c.731A=	NP_001005742.1:p.Tyr244=
NM_001171811.1:c.470A=	NP_001165282.1:p.Tyr157=
NM_001171812.1:c.584A=	NP_001165283.1:p.Tyr195=
XM_006711270.1:c.731A=	XP_006711333.1:p.Tyr244=
XM_011509407.1:c.731A=	XP_011507709.1:p.Tyr244=
NM_000157.4:c.731A= MANE Select	NP_000148.2:p.Tyr244=
NM_001005741.3:c.731A=	NP_001005741.1:p.Tyr244=
NM_001005742.3:c.731A=	NP_001005742.1:p.Tyr244=
NM_001171811.2:c.470A=	NP_001165282.1:p.Tyr157=
NM_001171812.2:c.584A=	NP_001165283.1:p.Tyr195=