Canonical Allele Identifier: CA2481203342
Gene: GBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155239553_155239558delinsAAAAAG , CM000663.2:g.155239553_155239558delinsAAAAAG GRCh38
NC_000001.10:g.155209344_155209349delinsAAAAAG , CM000663.1:g.155209344_155209349delinsAAAAAG GRCh37
NC_000001.9:g.153475968_153475973delinsAAAAAG NCBI36
NG_009783.1:g.10140_10145delinsCTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368373.8:c.454+58_454+63delinsCTTTTT MANE Select ENSP00000357357.3:n.454+58_454+63delinsCTTTTT
ENST00000327247.9:c.454+58_454+63delinsCTTTTT ENSP00000314508.5:n.454+58_454+63delinsCTTTTT
ENST00000368373.7:c.454+58_454+63delinsCTTTTT ENSP00000357357.3:n.454+58_454+63delinsCTTTTT
ENST00000427500.7:c.307+328_307+333delinsCTTTTT ENSP00000402577.2:n.307+328_307+333delinsCTTTTT
ENST00000428024.3:c.193+58_193+63delinsCTTTTT ENSP00000397986.2:n.193+58_193+63delinsCTTTTT
ENST00000473570.5:n.775+58_775+63delinsCTTTTT
ENST00000484489.5:n.339+415_339+420delinsCTTTTT
ENST00000493842.5:n.792+58_792+63delinsCTTTTT
ENST00000497670.5:n.77+328_77+333delinsCTTTTT
NM_000157.3:c.454+58_454+63delinsCTTTTT NP_000148.2:n.454+58_454+63delinsCTTTTT
NM_001005741.2:c.454+58_454+63delinsCTTTTT NP_001005741.1:n.454+58_454+63delinsCTTTTT
NM_001005742.2:c.454+58_454+63delinsCTTTTT NP_001005742.1:n.454+58_454+63delinsCTTTTT
NM_001171811.1:c.193+58_193+63delinsCTTTTT NP_001165282.1:n.193+58_193+63delinsCTTTTT
NM_001171812.1:c.307+328_307+333delinsCTTTTT NP_001165283.1:n.307+328_307+333delinsCTTTTT
XM_006711270.1:c.454+58_454+63delinsCTTTTT XP_006711333.1:n.454+58_454+63delinsCTTTTT
XM_011509407.1:c.454+58_454+63delinsCTTTTT XP_011507709.1:n.454+58_454+63delinsCTTTTT
NM_000157.4:c.454+58_454+63delinsCTTTTT MANE Select NP_000148.2:n.454+58_454+63delinsCTTTTT
NM_001005741.3:c.454+58_454+63delinsCTTTTT NP_001005741.1:n.454+58_454+63delinsCTTTTT
NM_001005742.3:c.454+58_454+63delinsCTTTTT NP_001005742.1:n.454+58_454+63delinsCTTTTT
NM_001171811.2:c.193+58_193+63delinsCTTTTT NP_001165282.1:n.193+58_193+63delinsCTTTTT
NM_001171812.2:c.307+328_307+333delinsCTTTTT NP_001165283.1:n.307+328_307+333delinsCTTTTT