Canonical Allele Identifier: CA341575

Gene: GBA1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155235843T>G , CM000663.2:g.155235843T>G	GRCh38
NC_000001.10:g.155205634T>G , CM000663.1:g.155205634T>G	GRCh37
NC_000001.9:g.153472258T>G	NCBI36
NG_009783.1:g.13855A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.1226A>C MANE Select	ENSP00000357357.3:p.Asn409Thr
ENST00000327247.9:c.1226A>C	ENSP00000314508.5:p.Asn409Thr
ENST00000368373.7:c.1226A>C	ENSP00000357357.3:p.Asn409Thr
ENST00000427500.7:c.1079A>C	ENSP00000402577.2:p.Asn360Thr
ENST00000428024.3:c.965A>C	ENSP00000397986.2:p.Asn322Thr
ENST00000478472.1:n.217A>C
ENST00000484489.5:n.385A>C
NM_000157.3:c.1226A>C	NP_000148.2:p.Asn409Thr
NM_001005741.2:c.1226A>C	NP_001005741.1:p.Asn409Thr
NM_001005742.2:c.1226A>C	NP_001005742.1:p.Asn409Thr
NM_001171811.1:c.965A>C	NP_001165282.1:p.Asn322Thr
NM_001171812.1:c.1079A>C	NP_001165283.1:p.Asn360Thr
XM_006711270.1:c.1226A>C	XP_006711333.1:p.Asn409Thr
XM_011509407.1:c.1226A>C	XP_011507709.1:p.Asn409Thr
NM_000157.4:c.1226A>C MANE Select	NP_000148.2:p.Asn409Thr
NM_001005741.3:c.1226A>C	NP_001005741.1:p.Asn409Thr
NM_001005742.3:c.1226A>C	NP_001005742.1:p.Asn409Thr
NM_001171811.2:c.965A>C	NP_001165282.1:p.Asn322Thr
NM_001171812.2:c.1079A>C	NP_001165283.1:p.Asn360Thr