Canonical Allele Identifier: CA1139792770
Gene: GBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155235217C= , CM000663.2:g.155235217C= GRCh38
NC_000001.10:g.155205008C= , CM000663.1:g.155205008C= GRCh37
NC_000001.9:g.153471632C= NCBI36
NG_009783.1:g.14481G=

Transcript Alleles

HGVS Amino-acid change
ENST00000368373.8:c.1483G= MANE Select ENSP00000357357.3:p.Ala495=
ENST00000327247.9:c.1483G= ENSP00000314508.5:p.Ala495=
ENST00000368373.7:c.1483G= ENSP00000357357.3:p.Ala495=
ENST00000427500.7:c.1336G= ENSP00000402577.2:p.Ala446=
ENST00000428024.3:c.1222G= ENSP00000397986.2:p.Ala408=
ENST00000464536.1:n.191-396G=
ENST00000478472.1:n.843G=
ENST00000484489.5:n.642G=
NM_000157.3:c.1483G= NP_000148.2:p.Ala495=
NM_001005741.2:c.1483G= NP_001005741.1:p.Ala495=
NM_001005742.2:c.1483G= NP_001005742.1:p.Ala495=
NM_001171811.1:c.1222G= NP_001165282.1:p.Ala408=
NM_001171812.1:c.1336G= NP_001165283.1:p.Ala446=
XM_006711270.1:c.1483G= XP_006711333.1:p.Ala495=
XM_011509407.1:c.1483G= XP_011507709.1:p.Ala495=
NM_000157.4:c.1483G= MANE Select NP_000148.2:p.Ala495=
NM_001005741.3:c.1483G= NP_001005741.1:p.Ala495=
NM_001005742.3:c.1483G= NP_001005742.1:p.Ala495=
NM_001171811.2:c.1222G= NP_001165282.1:p.Ala408=
NM_001171812.2:c.1336G= NP_001165283.1:p.Ala446=