Canonical Allele Identifier: CA342722163

Gene: GBA1

Linked Data

• dbSNP Id: rs1051872176
• gnomAD v4: 1-155238218-G-A
• MyVariant Identifiers: chr1:g.155208009G>A (hg19) ; chr1:g.155238218G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238218G>A , CM000663.2:g.155238218G>A	GRCh38
NC_000001.10:g.155208009G>A , CM000663.1:g.155208009G>A	GRCh37
NC_000001.9:g.153474633G>A	NCBI36
NG_009783.1:g.11480C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.677C>T MANE Select	ENSP00000357357.3:p.Thr226Ile
ENST00000327247.9:c.677C>T	ENSP00000314508.5:p.Thr226Ile
ENST00000368373.7:c.677C>T	ENSP00000357357.3:p.Thr226Ile
ENST00000427500.7:c.530C>T	ENSP00000402577.2:p.Thr177Ile
ENST00000428024.3:c.416C>T	ENSP00000397986.2:p.Thr139Ile
ENST00000460156.1:n.464C>T
ENST00000484489.5:n.339+1755C>T
ENST00000491081.5:n.282C>T
ENST00000493842.5:n.1015C>T
ENST00000497670.5:n.300C>T
NM_000157.3:c.677C>T	NP_000148.2:p.Thr226Ile
NM_001005741.2:c.677C>T	NP_001005741.1:p.Thr226Ile
NM_001005742.2:c.677C>T	NP_001005742.1:p.Thr226Ile
NM_001171811.1:c.416C>T	NP_001165282.1:p.Thr139Ile
NM_001171812.1:c.530C>T	NP_001165283.1:p.Thr177Ile
XM_006711270.1:c.677C>T	XP_006711333.1:p.Thr226Ile
XM_011509407.1:c.677C>T	XP_011507709.1:p.Thr226Ile
NM_000157.4:c.677C>T MANE Select	NP_000148.2:p.Thr226Ile
NM_001005741.3:c.677C>T	NP_001005741.1:p.Thr226Ile
NM_001005742.3:c.677C>T	NP_001005742.1:p.Thr226Ile
NM_001171811.2:c.416C>T	NP_001165282.1:p.Thr139Ile
NM_001171812.2:c.530C>T	NP_001165283.1:p.Thr177Ile