Canonical Allele Identifier: CA421028193
Gene: GBA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.155209762A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155239971A>T , CM000663.2:g.155239971A>T GRCh38
NC_000001.10:g.155209762A>T , CM000663.1:g.155209762A>T GRCh37
NC_000001.9:g.153476386A>T NCBI36
NG_009783.1:g.9727T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368373.8:c.222T>A MANE Select ENSP00000357357.3:p.Gly74=
ENST00000327247.9:c.222T>A ENSP00000314508.5:p.Gly74=
ENST00000368373.7:c.222T>A ENSP00000357357.3:p.Gly74=
ENST00000427500.7:c.222T>A ENSP00000402577.2:p.Gly74=
ENST00000428024.3:c.-40T>A ENSP00000397986.2:n.-40T>A
ENST00000467918.5:n.421-9T>A
ENST00000470104.1:n.476T>A
ENST00000473570.5:n.543T>A
ENST00000484489.5:n.339+2T>A
ENST00000493842.5:n.560T>A
NM_000157.3:c.222T>A NP_000148.2:p.Gly74=
NM_001005741.2:c.222T>A NP_001005741.1:p.Gly74=
NM_001005742.2:c.222T>A NP_001005742.1:p.Gly74=
NM_001171811.1:c.-40T>A NP_001165282.1:n.-40T>A
NM_001171812.1:c.222T>A NP_001165283.1:p.Gly74=
XM_006711270.1:c.222T>A XP_006711333.1:p.Gly74=
XM_011509407.1:c.222T>A XP_011507709.1:p.Gly74=
NM_000157.4:c.222T>A MANE Select NP_000148.2:p.Gly74=
NM_001005741.3:c.222T>A NP_001005741.1:p.Gly74=
NM_001005742.3:c.222T>A NP_001005742.1:p.Gly74=
NM_001171811.2:c.-40T>A NP_001165282.1:n.-40T>A
NM_001171812.2:c.222T>A NP_001165283.1:p.Gly74=