Canonical Allele Identifier: CA10581619

Gene: GBA1

Linked Data

• ClinVar Variation Id: 236406
• ClinVar RCV Id: RCV000225413
• dbSNP Id: rs878853321
• MyVariant Identifiers: chr1:g.155207265C>G (hg19) ; chr1:g.155237474C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155237474C>G , CM000663.2:g.155237474C>G	GRCh38
NC_000001.10:g.155207265C>G , CM000663.1:g.155207265C>G	GRCh37
NC_000001.9:g.153473889C>G	NCBI36
NG_009783.1:g.12224G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.866G>C MANE Select	ENSP00000357357.3:p.Gly289Ala
ENST00000327247.9:c.866G>C	ENSP00000314508.5:p.Gly289Ala
ENST00000368373.7:c.866G>C	ENSP00000357357.3:p.Gly289Ala
ENST00000427500.7:c.719G>C	ENSP00000402577.2:p.Gly240Ala
ENST00000428024.3:c.605G>C	ENSP00000397986.2:p.Gly202Ala
ENST00000484489.5:n.340-1186G>C
ENST00000491081.5:n.471G>C
ENST00000497670.5:n.489G>C
NM_000157.3:c.866G>C	NP_000148.2:p.Gly289Ala
NM_001005741.2:c.866G>C	NP_001005741.1:p.Gly289Ala
NM_001005742.2:c.866G>C	NP_001005742.1:p.Gly289Ala
NM_001171811.1:c.605G>C	NP_001165282.1:p.Gly202Ala
NM_001171812.1:c.719G>C	NP_001165283.1:p.Gly240Ala
XM_006711270.1:c.866G>C	XP_006711333.1:p.Gly289Ala
XM_011509407.1:c.866G>C	XP_011507709.1:p.Gly289Ala
NM_000157.4:c.866G>C MANE Select	NP_000148.2:p.Gly289Ala
NM_001005741.3:c.866G>C	NP_001005741.1:p.Gly289Ala
NM_001005742.3:c.866G>C	NP_001005742.1:p.Gly289Ala
NM_001171811.2:c.605G>C	NP_001165282.1:p.Gly202Ala
NM_001171812.2:c.719G>C	NP_001165283.1:p.Gly240Ala