Canonical Allele Identifier: CA1141022356
Gene: GBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155238637G= , CM000663.2:g.155238637G= GRCh38
NC_000001.10:g.155208428G= , CM000663.1:g.155208428G= GRCh37
NC_000001.9:g.153475052G= NCBI36
NG_009783.1:g.11061C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368373.8:c.468C= MANE Select ENSP00000357357.3:p.Asn156=
ENST00000327247.9:c.468C= ENSP00000314508.5:p.Asn156=
ENST00000368373.7:c.468C= ENSP00000357357.3:p.Asn156=
ENST00000427500.7:c.321C= ENSP00000402577.2:p.Asn107=
ENST00000428024.3:c.207C= ENSP00000397986.2:p.Asn69=
ENST00000460156.1:n.255C=
ENST00000473570.5:n.789C=
ENST00000484489.5:n.339+1336C=
ENST00000491081.5:n.73C=
ENST00000493842.5:n.806C=
ENST00000497670.5:n.91C=
NM_000157.3:c.468C= NP_000148.2:p.Asn156=
NM_001005741.2:c.468C= NP_001005741.1:p.Asn156=
NM_001005742.2:c.468C= NP_001005742.1:p.Asn156=
NM_001171811.1:c.207C= NP_001165282.1:p.Asn69=
NM_001171812.1:c.321C= NP_001165283.1:p.Asn107=
XM_006711270.1:c.468C= XP_006711333.1:p.Asn156=
XM_011509407.1:c.468C= XP_011507709.1:p.Asn156=
NM_000157.4:c.468C= MANE Select NP_000148.2:p.Asn156=
NM_001005741.3:c.468C= NP_001005741.1:p.Asn156=
NM_001005742.3:c.468C= NP_001005742.1:p.Asn156=
NM_001171811.2:c.207C= NP_001165282.1:p.Asn69=
NM_001171812.2:c.321C= NP_001165283.1:p.Asn107=