Canonical Allele Identifier: CA342726496

Gene: GBA1

Linked Data

• MyVariant Identifiers: chr1:g.155209533G>T (hg19) ; chr1:g.155239742G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155239742G>T , CM000663.2:g.155239742G>T	GRCh38
NC_000001.10:g.155209533G>T , CM000663.1:g.155209533G>T	GRCh37
NC_000001.9:g.153476157G>T	NCBI36
NG_009783.1:g.9956C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.328C>A MANE Select	ENSP00000357357.3:p.Pro110Thr
ENST00000327247.9:c.328C>A	ENSP00000314508.5:p.Pro110Thr
ENST00000368373.7:c.328C>A	ENSP00000357357.3:p.Pro110Thr
ENST00000427500.7:c.307+144C>A	ENSP00000402577.2:n.307+144C>A
ENST00000428024.3:c.67C>A	ENSP00000397986.2:p.Pro23Thr
ENST00000467918.5:n.518C>A
ENST00000473570.5:n.649C>A
ENST00000484489.5:n.339+231C>A
ENST00000493842.5:n.666C>A
ENST00000497670.5:n.77+144C>A
NM_000157.3:c.328C>A	NP_000148.2:p.Pro110Thr
NM_001005741.2:c.328C>A	NP_001005741.1:p.Pro110Thr
NM_001005742.2:c.328C>A	NP_001005742.1:p.Pro110Thr
NM_001171811.1:c.67C>A	NP_001165282.1:p.Pro23Thr
NM_001171812.1:c.307+144C>A	NP_001165283.1:n.307+144C>A
XM_006711270.1:c.328C>A	XP_006711333.1:p.Pro110Thr
XM_011509407.1:c.328C>A	XP_011507709.1:p.Pro110Thr
NM_000157.4:c.328C>A MANE Select	NP_000148.2:p.Pro110Thr
NM_001005741.3:c.328C>A	NP_001005741.1:p.Pro110Thr
NM_001005742.3:c.328C>A	NP_001005742.1:p.Pro110Thr
NM_001171811.2:c.67C>A	NP_001165282.1:p.Pro23Thr
NM_001171812.2:c.307+144C>A	NP_001165283.1:n.307+144C>A