Canonical Allele Identifier: CA342709654

Gene: GBA1

Linked Data

• gnomAD v4: 1-155235011-A-G
• MyVariant Identifiers: chr1:g.155204802A>G (hg19) ; chr1:g.155235011A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155235011A>G , CM000663.2:g.155235011A>G	GRCh38
NC_000001.10:g.155204802A>G , CM000663.1:g.155204802A>G	GRCh37
NC_000001.9:g.153471426A>G	NCBI36
NG_009783.1:g.14687T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.1595T>C MANE Select	ENSP00000357357.3:p.Leu532Pro
ENST00000327247.9:c.1595T>C	ENSP00000314508.5:p.Leu532Pro
ENST00000368373.7:c.1595T>C	ENSP00000357357.3:p.Leu532Pro
ENST00000427500.7:c.1448T>C	ENSP00000402577.2:p.Leu483Pro
ENST00000428024.3:c.1334T>C	ENSP00000397986.2:p.Leu445Pro
ENST00000464536.1:n.191-190T>C
ENST00000478472.1:n.955T>C
NM_000157.3:c.1595T>C	NP_000148.2:p.Leu532Pro
NM_001005741.2:c.1595T>C	NP_001005741.1:p.Leu532Pro
NM_001005742.2:c.1595T>C	NP_001005742.1:p.Leu532Pro
NM_001171811.1:c.1334T>C	NP_001165282.1:p.Leu445Pro
NM_001171812.1:c.1448T>C	NP_001165283.1:p.Leu483Pro
XM_006711270.1:c.1595T>C	XP_006711333.1:p.Leu532Pro
XM_011509407.1:c.1595T>C	XP_011507709.1:p.Leu532Pro
NM_000157.4:c.1595T>C MANE Select	NP_000148.2:p.Leu532Pro
NM_001005741.3:c.1595T>C	NP_001005741.1:p.Leu532Pro
NM_001005742.3:c.1595T>C	NP_001005742.1:p.Leu532Pro
NM_001171811.2:c.1334T>C	NP_001165282.1:p.Leu445Pro
NM_001171812.2:c.1448T>C	NP_001165283.1:p.Leu483Pro