Canonical Allele Identifier: CA2586967507
Gene: GBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155239934del , CM000663.2:g.155239934del GRCh38
NC_000001.10:g.155209725del , CM000663.1:g.155209725del GRCh37
NC_000001.9:g.153476349del NCBI36
NG_009783.1:g.9764del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368373.8:c.259del MANE Select ENSP00000357357.3:p.Arg87GlyfsTer4
ENST00000327247.9:c.259del ENSP00000314508.5:p.Arg87GlyfsTer4
ENST00000368373.7:c.259del ENSP00000357357.3:p.Arg87GlyfsTer4
ENST00000427500.7:c.259del ENSP00000402577.2:p.Arg87GlyfsTer4
ENST00000428024.3:c.-3del ENSP00000397986.2:n.-3del
ENST00000467918.5:n.449del
ENST00000473570.5:n.580del
ENST00000484489.5:n.339+39del
ENST00000493842.5:n.597del
ENST00000497670.5:n.29del
NM_000157.3:c.259del NP_000148.2:p.Arg87GlyfsTer4
NM_001005741.2:c.259del NP_001005741.1:p.Arg87GlyfsTer4
NM_001005742.2:c.259del NP_001005742.1:p.Arg87GlyfsTer4
NM_001171811.1:c.-3del NP_001165282.1:n.-3del
NM_001171812.1:c.259del NP_001165283.1:p.Arg87GlyfsTer4
XM_006711270.1:c.259del XP_006711333.1:p.Arg87GlyfsTer4
XM_011509407.1:c.259del XP_011507709.1:p.Arg87GlyfsTer4
NM_000157.4:c.259del MANE Select NP_000148.2:p.Arg87GlyfsTer4
NM_001005741.3:c.259del NP_001005741.1:p.Arg87GlyfsTer4
NM_001005742.3:c.259del NP_001005742.1:p.Arg87GlyfsTer4
NM_001171811.2:c.-3del NP_001165282.1:n.-3del
NM_001171812.2:c.259del NP_001165283.1:p.Arg87GlyfsTer4