Canonical Allele Identifier: CA2481203710
Gene: GBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155239943T= , CM000663.2:g.155239943T= GRCh38
NC_000001.10:g.155209734T= , CM000663.1:g.155209734T= GRCh37
NC_000001.9:g.153476358T= NCBI36
NG_009783.1:g.9755A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368373.8:c.250A= MANE Select ENSP00000357357.3:p.Ser84=
ENST00000327247.9:c.250A= ENSP00000314508.5:p.Ser84=
ENST00000368373.7:c.250A= ENSP00000357357.3:p.Ser84=
ENST00000427500.7:c.250A= ENSP00000402577.2:p.Ser84=
ENST00000428024.3:c.-12A= ENSP00000397986.2:n.-12A=
ENST00000467918.5:n.440A=
ENST00000473570.5:n.571A=
ENST00000484489.5:n.339+30A=
ENST00000493842.5:n.588A=
ENST00000497670.5:n.20A=
NM_000157.3:c.250A= NP_000148.2:p.Ser84=
NM_001005741.2:c.250A= NP_001005741.1:p.Ser84=
NM_001005742.2:c.250A= NP_001005742.1:p.Ser84=
NM_001171811.1:c.-12A= NP_001165282.1:n.-12A=
NM_001171812.1:c.250A= NP_001165283.1:p.Ser84=
XM_006711270.1:c.250A= XP_006711333.1:p.Ser84=
XM_011509407.1:c.250A= XP_011507709.1:p.Ser84=
NM_000157.4:c.250A= MANE Select NP_000148.2:p.Ser84=
NM_001005741.3:c.250A= NP_001005741.1:p.Ser84=
NM_001005742.3:c.250A= NP_001005742.1:p.Ser84=
NM_001171811.2:c.-12A= NP_001165282.1:n.-12A=
NM_001171812.2:c.250A= NP_001165283.1:p.Ser84=