Canonical Allele Identifier: CA342724797

Gene: GBA1

Linked Data

• MyVariant Identifiers: chr1:g.155208424T>C (hg19) ; chr1:g.155238633T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238633T>C , CM000663.2:g.155238633T>C	GRCh38
NC_000001.10:g.155208424T>C , CM000663.1:g.155208424T>C	GRCh37
NC_000001.9:g.153475048T>C	NCBI36
NG_009783.1:g.11065A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368373.8:c.472A>G MANE Select	ENSP00000357357.3:p.Ile158Val
ENST00000327247.9:c.472A>G	ENSP00000314508.5:p.Ile158Val
ENST00000368373.7:c.472A>G	ENSP00000357357.3:p.Ile158Val
ENST00000427500.7:c.325A>G	ENSP00000402577.2:p.Ile109Val
ENST00000428024.3:c.211A>G	ENSP00000397986.2:p.Ile71Val
ENST00000460156.1:n.259A>G
ENST00000473570.5:n.793A>G
ENST00000484489.5:n.339+1340A>G
ENST00000491081.5:n.77A>G
ENST00000493842.5:n.810A>G
ENST00000497670.5:n.95A>G
NM_000157.3:c.472A>G	NP_000148.2:p.Ile158Val
NM_001005741.2:c.472A>G	NP_001005741.1:p.Ile158Val
NM_001005742.2:c.472A>G	NP_001005742.1:p.Ile158Val
NM_001171811.1:c.211A>G	NP_001165282.1:p.Ile71Val
NM_001171812.1:c.325A>G	NP_001165283.1:p.Ile109Val
XM_006711270.1:c.472A>G	XP_006711333.1:p.Ile158Val
XM_011509407.1:c.472A>G	XP_011507709.1:p.Ile158Val
NM_000157.4:c.472A>G MANE Select	NP_000148.2:p.Ile158Val
NM_001005741.3:c.472A>G	NP_001005741.1:p.Ile158Val
NM_001005742.3:c.472A>G	NP_001005742.1:p.Ile158Val
NM_001171811.2:c.211A>G	NP_001165282.1:p.Ile71Val
NM_001171812.2:c.325A>G	NP_001165283.1:p.Ile109Val