Canonical Allele Identifier: CA2481202710

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238065G= , CM000663.2:g.155238065G=	GRCh38
NC_000001.10:g.155207856G= , CM000663.1:g.155207856G=	GRCh37
NC_000001.9:g.153474480G=	NCBI36
NG_009783.1:g.11633C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.761+69C= MANE Select	ENSP00000357357.3:n.761+69C=
ENST00000327247.9:c.761+69C=	ENSP00000314508.5:n.761+69C=
ENST00000368373.7:c.761+69C=	ENSP00000357357.3:n.761+69C=
ENST00000427500.7:c.614+69C=	ENSP00000402577.2:n.614+69C=
ENST00000428024.3:c.500+69C=	ENSP00000397986.2:n.500+69C=
ENST00000460156.1:n.617C=
ENST00000484489.5:n.340-1777C=
ENST00000491081.5:n.366+69C=
ENST00000497670.5:n.384+69C=
NM_000157.3:c.761+69C=	NP_000148.2:n.761+69C=
NM_001005741.2:c.761+69C=	NP_001005741.1:n.761+69C=
NM_001005742.2:c.761+69C=	NP_001005742.1:n.761+69C=
NM_001171811.1:c.500+69C=	NP_001165282.1:n.500+69C=
NM_001171812.1:c.614+69C=	NP_001165283.1:n.614+69C=
XM_006711270.1:c.761+69C=	XP_006711333.1:n.761+69C=
XM_011509407.1:c.761+69C=	XP_011507709.1:n.761+69C=
NM_000157.4:c.761+69C= MANE Select	NP_000148.2:n.761+69C=
NM_001005741.3:c.761+69C=	NP_001005741.1:n.761+69C=
NM_001005742.3:c.761+69C=	NP_001005742.1:n.761+69C=
NM_001171811.2:c.500+69C=	NP_001165282.1:n.500+69C=
NM_001171812.2:c.614+69C=	NP_001165283.1:n.614+69C=