Canonical Allele Identifier: CA2648253681
Gene: GBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155239866del , CM000663.2:g.155239866del GRCh38
NC_000001.10:g.155209657del , CM000663.1:g.155209657del GRCh37
NC_000001.9:g.153476281del NCBI36
NG_009783.1:g.9836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368373.8:c.307+24del MANE Select ENSP00000357357.3:n.307+24del
ENST00000327247.9:c.307+24del ENSP00000314508.5:n.307+24del
ENST00000368373.7:c.307+24del ENSP00000357357.3:n.307+24del
ENST00000427500.7:c.307+24del ENSP00000402577.2:n.307+24del
ENST00000428024.3:c.46+24del ENSP00000397986.2:n.46+24del
ENST00000467918.5:n.497+24del
ENST00000473570.5:n.628+24del
ENST00000484489.5:n.339+111del
ENST00000493842.5:n.645+24del
ENST00000497670.5:n.77+24del
NM_000157.3:c.307+24del NP_000148.2:n.307+24del
NM_001005741.2:c.307+24del NP_001005741.1:n.307+24del
NM_001005742.2:c.307+24del NP_001005742.1:n.307+24del
NM_001171811.1:c.46+24del NP_001165282.1:n.46+24del
NM_001171812.1:c.307+24del NP_001165283.1:n.307+24del
XM_006711270.1:c.307+24del XP_006711333.1:n.307+24del
XM_011509407.1:c.307+24del XP_011507709.1:n.307+24del
NM_000157.4:c.307+24del MANE Select NP_000148.2:n.307+24del
NM_001005741.3:c.307+24del NP_001005741.1:n.307+24del
NM_001005742.3:c.307+24del NP_001005742.1:n.307+24del
NM_001171811.2:c.46+24del NP_001165282.1:n.46+24del
NM_001171812.2:c.307+24del NP_001165283.1:n.307+24del