Canonical Allele Identifier: CA2481202886
Gene: GBA1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000368373.8:c.566C= MANE Select ENSP00000357357.3:p.Pro189=
ENST00000327247.9:c.566C= ENSP00000314508.5:p.Pro189=
ENST00000368373.7:c.566C= ENSP00000357357.3:p.Pro189=
ENST00000427500.7:c.419C= ENSP00000402577.2:p.Pro140=
ENST00000428024.3:c.305C= ENSP00000397986.2:p.Pro102=
ENST00000460156.1:n.353C=
ENST00000484489.5:n.339+1434C=
ENST00000491081.5:n.171C=
ENST00000493842.5:n.904C=
ENST00000497670.5:n.189C=
NM_000157.3:c.566C= NP_000148.2:p.Pro189=
NM_001005741.2:c.566C= NP_001005741.1:p.Pro189=
NM_001005742.2:c.566C= NP_001005742.1:p.Pro189=
NM_001171811.1:c.305C= NP_001165282.1:p.Pro102=
NM_001171812.1:c.419C= NP_001165283.1:p.Pro140=
XM_006711270.1:c.566C= XP_006711333.1:p.Pro189=
XM_011509407.1:c.566C= XP_011507709.1:p.Pro189=
NM_000157.4:c.566C= MANE Select NP_000148.2:p.Pro189=
NM_001005741.3:c.566C= NP_001005741.1:p.Pro189=
NM_001005742.3:c.566C= NP_001005742.1:p.Pro189=
NM_001171811.2:c.305C= NP_001165282.1:p.Pro102=
NM_001171812.2:c.419C= NP_001165283.1:p.Pro140=