Canonical Allele Identifier: CA1143566979

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155237458A= , CM000663.2:g.155237458A=	GRCh38
NC_000001.10:g.155207249A= , CM000663.1:g.155207249A=	GRCh37
NC_000001.9:g.153473873A=	NCBI36
NG_009783.1:g.12240T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.882T= MANE Select	ENSP00000357357.3:p.His294=
ENST00000327247.9:c.882T=	ENSP00000314508.5:p.His294=
ENST00000368373.7:c.882T=	ENSP00000357357.3:p.His294=
ENST00000427500.7:c.735T=	ENSP00000402577.2:p.His245=
ENST00000428024.3:c.621T=	ENSP00000397986.2:p.His207=
ENST00000484489.5:n.340-1170T=
ENST00000491081.5:n.487T=
ENST00000497670.5:n.505T=
NM_000157.3:c.882T=	NP_000148.2:p.His294=
NM_001005741.2:c.882T=	NP_001005741.1:p.His294=
NM_001005742.2:c.882T=	NP_001005742.1:p.His294=
NM_001171811.1:c.621T=	NP_001165282.1:p.His207=
NM_001171812.1:c.735T=	NP_001165283.1:p.His245=
XM_006711270.1:c.882T=	XP_006711333.1:p.His294=
XM_011509407.1:c.882T=	XP_011507709.1:p.His294=
NM_000157.4:c.882T= MANE Select	NP_000148.2:p.His294=
NM_001005741.3:c.882T=	NP_001005741.1:p.His294=
NM_001005742.3:c.882T=	NP_001005742.1:p.His294=
NM_001171811.2:c.621T=	NP_001165282.1:p.His207=
NM_001171812.2:c.735T=	NP_001165283.1:p.His245=