Canonical Allele Identifier: CA421026530
Gene: GBA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.155208434T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155238643T>C , CM000663.2:g.155238643T>C GRCh38
NC_000001.10:g.155208434T>C , CM000663.1:g.155208434T>C GRCh37
NC_000001.9:g.153475058T>C NCBI36
NG_009783.1:g.11055A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368373.8:c.462A>G MANE Select ENSP00000357357.3:p.Gly154=
ENST00000327247.9:c.462A>G ENSP00000314508.5:p.Gly154=
ENST00000368373.7:c.462A>G ENSP00000357357.3:p.Gly154=
ENST00000427500.7:c.315A>G ENSP00000402577.2:p.Gly105=
ENST00000428024.3:c.201A>G ENSP00000397986.2:p.Gly67=
ENST00000460156.1:n.249A>G
ENST00000473570.5:n.783A>G
ENST00000484489.5:n.339+1330A>G
ENST00000491081.5:n.67A>G
ENST00000493842.5:n.800A>G
ENST00000497670.5:n.85A>G
NM_000157.3:c.462A>G NP_000148.2:p.Gly154=
NM_001005741.2:c.462A>G NP_001005741.1:p.Gly154=
NM_001005742.2:c.462A>G NP_001005742.1:p.Gly154=
NM_001171811.1:c.201A>G NP_001165282.1:p.Gly67=
NM_001171812.1:c.315A>G NP_001165283.1:p.Gly105=
XM_006711270.1:c.462A>G XP_006711333.1:p.Gly154=
XM_011509407.1:c.462A>G XP_011507709.1:p.Gly154=
NM_000157.4:c.462A>G MANE Select NP_000148.2:p.Gly154=
NM_001005741.3:c.462A>G NP_001005741.1:p.Gly154=
NM_001005742.3:c.462A>G NP_001005742.1:p.Gly154=
NM_001171811.2:c.201A>G NP_001165282.1:p.Gly67=
NM_001171812.2:c.315A>G NP_001165283.1:p.Gly105=