Canonical Allele Identifier: CA2648253391
Gene: GBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155239754del , CM000663.2:g.155239754del GRCh38
NC_000001.10:g.155209545del , CM000663.1:g.155209545del GRCh37
NC_000001.9:g.153476169del NCBI36
NG_009783.1:g.9944del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368373.8:c.316del MANE Select ENSP00000357357.3:p.Leu106Ter
ENST00000327247.9:c.316del ENSP00000314508.5:p.Leu106Ter
ENST00000368373.7:c.316del ENSP00000357357.3:p.Leu106Ter
ENST00000427500.7:c.307+132del ENSP00000402577.2:n.307+132del
ENST00000428024.3:c.55del ENSP00000397986.2:p.Leu19Ter
ENST00000467918.5:n.506del
ENST00000473570.5:n.637del
ENST00000484489.5:n.339+219del
ENST00000493842.5:n.654del
ENST00000497670.5:n.77+132del
NM_000157.3:c.316del NP_000148.2:p.Leu106Ter
NM_001005741.2:c.316del NP_001005741.1:p.Leu106Ter
NM_001005742.2:c.316del NP_001005742.1:p.Leu106Ter
NM_001171811.1:c.55del NP_001165282.1:p.Leu19Ter
NM_001171812.1:c.307+132del NP_001165283.1:n.307+132del
XM_006711270.1:c.316del XP_006711333.1:p.Leu106Ter
XM_011509407.1:c.316del XP_011507709.1:p.Leu106Ter
NM_000157.4:c.316del MANE Select NP_000148.2:p.Leu106Ter
NM_001005741.3:c.316del NP_001005741.1:p.Leu106Ter
NM_001005742.3:c.316del NP_001005742.1:p.Leu106Ter
NM_001171811.2:c.55del NP_001165282.1:p.Leu19Ter
NM_001171812.2:c.307+132del NP_001165283.1:n.307+132del