Canonical Allele Identifier: CA10581620

Gene: GBA1

Linked Data

• ClinVar Variation Id: 236399
• ClinVar RCV Id: RCV000225581
• dbSNP Id: rs878853314
• MyVariant Identifiers: chr1:g.155209446C>G (hg19) ; chr1:g.155239655C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155239655C>G , CM000663.2:g.155239655C>G	GRCh38
NC_000001.10:g.155209446C>G , CM000663.1:g.155209446C>G	GRCh37
NC_000001.9:g.153476070C>G	NCBI36
NG_009783.1:g.10043G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.415G>C MANE Select	ENSP00000357357.3:p.Ala139Pro
ENST00000327247.9:c.415G>C	ENSP00000314508.5:p.Ala139Pro
ENST00000368373.7:c.415G>C	ENSP00000357357.3:p.Ala139Pro
ENST00000427500.7:c.307+231G>C	ENSP00000402577.2:n.307+231G>C
ENST00000428024.3:c.154G>C	ENSP00000397986.2:p.Ala52Pro
ENST00000467918.5:n.605G>C
ENST00000473570.5:n.736G>C
ENST00000484489.5:n.339+318G>C
ENST00000493842.5:n.753G>C
ENST00000497670.5:n.77+231G>C
NM_000157.3:c.415G>C	NP_000148.2:p.Ala139Pro
NM_001005741.2:c.415G>C	NP_001005741.1:p.Ala139Pro
NM_001005742.2:c.415G>C	NP_001005742.1:p.Ala139Pro
NM_001171811.1:c.154G>C	NP_001165282.1:p.Ala52Pro
NM_001171812.1:c.307+231G>C	NP_001165283.1:n.307+231G>C
XM_006711270.1:c.415G>C	XP_006711333.1:p.Ala139Pro
XM_011509407.1:c.415G>C	XP_011507709.1:p.Ala139Pro
NM_000157.4:c.415G>C MANE Select	NP_000148.2:p.Ala139Pro
NM_001005741.3:c.415G>C	NP_001005741.1:p.Ala139Pro
NM_001005742.3:c.415G>C	NP_001005742.1:p.Ala139Pro
NM_001171811.2:c.154G>C	NP_001165282.1:p.Ala52Pro
NM_001171812.2:c.307+231G>C	NP_001165283.1:n.307+231G>C