Canonical Allele Identifier: CA1141795

Gene: GBA1

Linked Data

• dbSNP Id: rs778349378
• ExAC: 1:155209681 G / T
• gnomAD v2: 1-155209681-G-T
• gnomAD v4: 1-155239890-G-T
• MyVariant Identifiers: chr1:g.155209681G>T (hg19) ; chr1:g.155239890G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155239890G>T , CM000663.2:g.155239890G>T	GRCh38
NC_000001.10:g.155209681G>T , CM000663.1:g.155209681G>T	GRCh37
NC_000001.9:g.153476305G>T	NCBI36
NG_009783.1:g.9808C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.303C>A MANE Select	ENSP00000357357.3:p.Gly101=
ENST00000327247.9:c.303C>A	ENSP00000314508.5:p.Gly101=
ENST00000368373.7:c.303C>A	ENSP00000357357.3:p.Gly101=
ENST00000427500.7:c.303C>A	ENSP00000402577.2:p.Gly101=
ENST00000428024.3:c.42C>A	ENSP00000397986.2:p.Gly14=
ENST00000467918.5:n.493C>A
ENST00000473570.5:n.624C>A
ENST00000484489.5:n.339+83C>A
ENST00000493842.5:n.641C>A
ENST00000497670.5:n.73C>A
NM_000157.3:c.303C>A	NP_000148.2:p.Gly101=
NM_001005741.2:c.303C>A	NP_001005741.1:p.Gly101=
NM_001005742.2:c.303C>A	NP_001005742.1:p.Gly101=
NM_001171811.1:c.42C>A	NP_001165282.1:p.Gly14=
NM_001171812.1:c.303C>A	NP_001165283.1:p.Gly101=
XM_006711270.1:c.303C>A	XP_006711333.1:p.Gly101=
XM_011509407.1:c.303C>A	XP_011507709.1:p.Gly101=
NM_000157.4:c.303C>A MANE Select	NP_000148.2:p.Gly101=
NM_001005741.3:c.303C>A	NP_001005741.1:p.Gly101=
NM_001005742.3:c.303C>A	NP_001005742.1:p.Gly101=
NM_001171811.2:c.42C>A	NP_001165282.1:p.Gly14=
NM_001171812.2:c.303C>A	NP_001165283.1:p.Gly101=