Canonical Allele Identifier: CA342723758
Gene: GBA1 HGNC NCBI

Linked Data

dbSNP Id: rs1421091684

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155238539G>A , CM000663.2:g.155238539G>A GRCh38
NC_000001.10:g.155208330G>A , CM000663.1:g.155208330G>A GRCh37
NC_000001.9:g.153474954G>A NCBI36
NG_009783.1:g.11159C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368373.8:c.566C>T MANE Select ENSP00000357357.3:p.Pro189Leu
ENST00000327247.9:c.566C>T ENSP00000314508.5:p.Pro189Leu
ENST00000368373.7:c.566C>T ENSP00000357357.3:p.Pro189Leu
ENST00000427500.7:c.419C>T ENSP00000402577.2:p.Pro140Leu
ENST00000428024.3:c.305C>T ENSP00000397986.2:p.Pro102Leu
ENST00000460156.1:n.353C>T
ENST00000484489.5:n.339+1434C>T
ENST00000491081.5:n.171C>T
ENST00000493842.5:n.904C>T
ENST00000497670.5:n.189C>T
NM_000157.3:c.566C>T NP_000148.2:p.Pro189Leu
NM_001005741.2:c.566C>T NP_001005741.1:p.Pro189Leu
NM_001005742.2:c.566C>T NP_001005742.1:p.Pro189Leu
NM_001171811.1:c.305C>T NP_001165282.1:p.Pro102Leu
NM_001171812.1:c.419C>T NP_001165283.1:p.Pro140Leu
XM_006711270.1:c.566C>T XP_006711333.1:p.Pro189Leu
XM_011509407.1:c.566C>T XP_011507709.1:p.Pro189Leu
NM_000157.4:c.566C>T MANE Select NP_000148.2:p.Pro189Leu
NM_001005741.3:c.566C>T NP_001005741.1:p.Pro189Leu
NM_001005742.3:c.566C>T NP_001005742.1:p.Pro189Leu
NM_001171811.2:c.305C>T NP_001165282.1:p.Pro102Leu
NM_001171812.2:c.419C>T NP_001165283.1:p.Pro140Leu