Canonical Allele Identifier: CA421025571
Gene: GBA1 HGNC NCBI

Linked Data

dbSNP Id: rs1423274387

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155238163G>A , CM000663.2:g.155238163G>A GRCh38
NC_000001.10:g.155207954G>A , CM000663.1:g.155207954G>A GRCh37
NC_000001.9:g.153474578G>A NCBI36
NG_009783.1:g.11535C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368373.8:c.732C>T MANE Select ENSP00000357357.3:p.Tyr244=
ENST00000327247.9:c.732C>T ENSP00000314508.5:p.Tyr244=
ENST00000368373.7:c.732C>T ENSP00000357357.3:p.Tyr244=
ENST00000427500.7:c.585C>T ENSP00000402577.2:p.Tyr195=
ENST00000428024.3:c.471C>T ENSP00000397986.2:p.Tyr157=
ENST00000460156.1:n.519C>T
ENST00000484489.5:n.339+1810C>T
ENST00000491081.5:n.337C>T
ENST00000497670.5:n.355C>T
NM_000157.3:c.732C>T NP_000148.2:p.Tyr244=
NM_001005741.2:c.732C>T NP_001005741.1:p.Tyr244=
NM_001005742.2:c.732C>T NP_001005742.1:p.Tyr244=
NM_001171811.1:c.471C>T NP_001165282.1:p.Tyr157=
NM_001171812.1:c.585C>T NP_001165283.1:p.Tyr195=
XM_006711270.1:c.732C>T XP_006711333.1:p.Tyr244=
XM_011509407.1:c.732C>T XP_011507709.1:p.Tyr244=
NM_000157.4:c.732C>T MANE Select NP_000148.2:p.Tyr244=
NM_001005741.3:c.732C>T NP_001005741.1:p.Tyr244=
NM_001005742.3:c.732C>T NP_001005742.1:p.Tyr244=
NM_001171811.2:c.471C>T NP_001165282.1:p.Tyr157=
NM_001171812.2:c.585C>T NP_001165283.1:p.Tyr195=