Canonical Allele Identifier: CA342724725

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238626A>G , CM000663.2:g.155238626A>G	GRCh38
NC_000001.10:g.155208417A>G , CM000663.1:g.155208417A>G	GRCh37
NC_000001.9:g.153475041A>G	NCBI36
NG_009783.1:g.11072T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000157.4:c.479T>C MANE Select	NP_000148.2:p.Val160Ala
ENST00000368373.8:c.479T>C MANE Select	ENSP00000357357.3:p.Val160Ala
NM_000157.3:c.479T>C	NP_000148.2:p.Val160Ala
NM_001005741.2:c.479T>C	NP_001005741.1:p.Val160Ala
NM_001005741.3:c.479T>C	NP_001005741.1:p.Val160Ala
NM_001005742.2:c.479T>C	NP_001005742.1:p.Val160Ala
NM_001005742.3:c.479T>C	NP_001005742.1:p.Val160Ala
NM_001171811.1:c.218T>C	NP_001165282.1:p.Val73Ala
NM_001171811.2:c.218T>C	NP_001165282.1:p.Val73Ala
NM_001171812.1:c.332T>C	NP_001165283.1:p.Val111Ala
NM_001171812.2:c.332T>C	NP_001165283.1:p.Val111Ala
ENST00000327247.9:c.479T>C	ENSP00000314508.5:p.Val160Ala
ENST00000368373.7:c.479T>C	ENSP00000357357.3:p.Val160Ala
ENST00000427500.7:c.332T>C	ENSP00000402577.2:p.Val111Ala
ENST00000428024.3:c.218T>C	ENSP00000397986.2:p.Val73Ala
ENST00000460156.1:n.266T>C
ENST00000473570.5:n.800T>C
ENST00000484489.5:n.339+1347T>C
ENST00000491081.5:n.84T>C
ENST00000493842.5:n.817T>C
ENST00000497670.5:n.102T>C
XM_006711270.1:c.479T>C	XP_006711333.1:p.Val160Ala
XM_011509407.1:c.479T>C	XP_011507709.1:p.Val160Ala