Canonical Allele Identifier: CA2481203636
Gene: GBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155239807_155239809delinsAAC , CM000663.2:g.155239807_155239809delinsAAC GRCh38
NC_000001.10:g.155209598_155209600delinsAAC , CM000663.1:g.155209598_155209600delinsAAC GRCh37
NC_000001.9:g.153476222_153476224delinsAAC NCBI36
NG_009783.1:g.9889_9891delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368373.8:c.308-47_308-45delinsGTT MANE Select ENSP00000357357.3:n.308-47_308-45delinsGTT
ENST00000327247.9:c.308-47_308-45delinsGTT ENSP00000314508.5:n.308-47_308-45delinsGTT
ENST00000368373.7:c.308-47_308-45delinsGTT ENSP00000357357.3:n.308-47_308-45delinsGTT
ENST00000427500.7:c.307+77_307+79delinsGTT ENSP00000402577.2:n.307+77_307+79delinsGTT
ENST00000428024.3:c.47-47_47-45delinsGTT ENSP00000397986.2:n.47-47_47-45delinsGTT
ENST00000467918.5:n.498-47_498-45delinsGTT
ENST00000473570.5:n.629-47_629-45delinsGTT
ENST00000484489.5:n.339+164_339+166delinsGTT
ENST00000493842.5:n.646-47_646-45delinsGTT
ENST00000497670.5:n.77+77_77+79delinsGTT
NM_000157.3:c.308-47_308-45delinsGTT NP_000148.2:n.308-47_308-45delinsGTT
NM_001005741.2:c.308-47_308-45delinsGTT NP_001005741.1:n.308-47_308-45delinsGTT
NM_001005742.2:c.308-47_308-45delinsGTT NP_001005742.1:n.308-47_308-45delinsGTT
NM_001171811.1:c.47-47_47-45delinsGTT NP_001165282.1:n.47-47_47-45delinsGTT
NM_001171812.1:c.307+77_307+79delinsGTT NP_001165283.1:n.307+77_307+79delinsGTT
XM_006711270.1:c.308-47_308-45delinsGTT XP_006711333.1:n.308-47_308-45delinsGTT
XM_011509407.1:c.308-47_308-45delinsGTT XP_011507709.1:n.308-47_308-45delinsGTT
NM_000157.4:c.308-47_308-45delinsGTT MANE Select NP_000148.2:n.308-47_308-45delinsGTT
NM_001005741.3:c.308-47_308-45delinsGTT NP_001005741.1:n.308-47_308-45delinsGTT
NM_001005742.3:c.308-47_308-45delinsGTT NP_001005742.1:n.308-47_308-45delinsGTT
NM_001171811.2:c.47-47_47-45delinsGTT NP_001165282.1:n.47-47_47-45delinsGTT
NM_001171812.2:c.307+77_307+79delinsGTT NP_001165283.1:n.307+77_307+79delinsGTT