Canonical Allele Identifier: CA2481202736

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238152C= , CM000663.2:g.155238152C=	GRCh38
NC_000001.10:g.155207943C= , CM000663.1:g.155207943C=	GRCh37
NC_000001.9:g.153474567C=	NCBI36
NG_009783.1:g.11546G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368373.8:c.743G= MANE Select	ENSP00000357357.3:p.Trp248=
ENST00000327247.9:c.743G=	ENSP00000314508.5:p.Trp248=
ENST00000368373.7:c.743G=	ENSP00000357357.3:p.Trp248=
ENST00000427500.7:c.596G=	ENSP00000402577.2:p.Trp199=
ENST00000428024.3:c.482G=	ENSP00000397986.2:p.Trp161=
ENST00000460156.1:n.530G=
ENST00000484489.5:n.339+1821G=
ENST00000491081.5:n.348G=
ENST00000497670.5:n.366G=
NM_000157.3:c.743G=	NP_000148.2:p.Trp248=
NM_001005741.2:c.743G=	NP_001005741.1:p.Trp248=
NM_001005742.2:c.743G=	NP_001005742.1:p.Trp248=
NM_001171811.1:c.482G=	NP_001165282.1:p.Trp161=
NM_001171812.1:c.596G=	NP_001165283.1:p.Trp199=
XM_006711270.1:c.743G=	XP_006711333.1:p.Trp248=
XM_011509407.1:c.743G=	XP_011507709.1:p.Trp248=
NM_000157.4:c.743G= MANE Select	NP_000148.2:p.Trp248=
NM_001005741.3:c.743G=	NP_001005741.1:p.Trp248=
NM_001005742.3:c.743G=	NP_001005742.1:p.Trp248=
NM_001171811.2:c.482G=	NP_001165282.1:p.Trp161=
NM_001171812.2:c.596G=	NP_001165283.1:p.Trp199=