Canonical Allele Identifier: CA421021883

Gene: GBA1

Linked Data

• MyVariant Identifiers: chr1:g.155206186T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155236395T>A , CM000663.2:g.155236395T>A	GRCh38
NC_000001.10:g.155206186T>A , CM000663.1:g.155206186T>A	GRCh37
NC_000001.9:g.153472810T>A	NCBI36
NG_009783.1:g.13303A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.1074A>T MANE Select	ENSP00000357357.3:p.Pro358=
ENST00000327247.9:c.1074A>T	ENSP00000314508.5:p.Pro358=
ENST00000368373.7:c.1074A>T	ENSP00000357357.3:p.Pro358=
ENST00000427500.7:c.927A>T	ENSP00000402577.2:p.Pro309=
ENST00000428024.3:c.813A>T	ENSP00000397986.2:p.Pro271=
ENST00000478472.1:n.65A>T
ENST00000484489.5:n.340-107A>T
ENST00000491081.5:n.679A>T
NM_000157.3:c.1074A>T	NP_000148.2:p.Pro358=
NM_001005741.2:c.1074A>T	NP_001005741.1:p.Pro358=
NM_001005742.2:c.1074A>T	NP_001005742.1:p.Pro358=
NM_001171811.1:c.813A>T	NP_001165282.1:p.Pro271=
NM_001171812.1:c.927A>T	NP_001165283.1:p.Pro309=
XM_006711270.1:c.1074A>T	XP_006711333.1:p.Pro358=
XM_011509407.1:c.1074A>T	XP_011507709.1:p.Pro358=
NM_000157.4:c.1074A>T MANE Select	NP_000148.2:p.Pro358=
NM_001005741.3:c.1074A>T	NP_001005741.1:p.Pro358=
NM_001005742.3:c.1074A>T	NP_001005742.1:p.Pro358=
NM_001171811.2:c.813A>T	NP_001165282.1:p.Pro271=
NM_001171812.2:c.927A>T	NP_001165283.1:p.Pro309=