Canonical Allele Identifier: CA421026080

Gene: GBA1

Linked Data

• MyVariant Identifiers: chr1:g.155208329T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238538T>G , CM000663.2:g.155238538T>G	GRCh38
NC_000001.10:g.155208329T>G , CM000663.1:g.155208329T>G	GRCh37
NC_000001.9:g.153474953T>G	NCBI36
NG_009783.1:g.11160A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368373.8:c.567A>C MANE Select	ENSP00000357357.3:p.Pro189=
ENST00000327247.9:c.567A>C	ENSP00000314508.5:p.Pro189=
ENST00000368373.7:c.567A>C	ENSP00000357357.3:p.Pro189=
ENST00000427500.7:c.420A>C	ENSP00000402577.2:p.Pro140=
ENST00000428024.3:c.306A>C	ENSP00000397986.2:p.Pro102=
ENST00000460156.1:n.354A>C
ENST00000484489.5:n.339+1435A>C
ENST00000491081.5:n.172A>C
ENST00000493842.5:n.905A>C
ENST00000497670.5:n.190A>C
NM_000157.3:c.567A>C	NP_000148.2:p.Pro189=
NM_001005741.2:c.567A>C	NP_001005741.1:p.Pro189=
NM_001005742.2:c.567A>C	NP_001005742.1:p.Pro189=
NM_001171811.1:c.306A>C	NP_001165282.1:p.Pro102=
NM_001171812.1:c.420A>C	NP_001165283.1:p.Pro140=
XM_006711270.1:c.567A>C	XP_006711333.1:p.Pro189=
XM_011509407.1:c.567A>C	XP_011507709.1:p.Pro189=
NM_000157.4:c.567A>C MANE Select	NP_000148.2:p.Pro189=
NM_001005741.3:c.567A>C	NP_001005741.1:p.Pro189=
NM_001005742.3:c.567A>C	NP_001005742.1:p.Pro189=
NM_001171811.2:c.306A>C	NP_001165282.1:p.Pro102=
NM_001171812.2:c.420A>C	NP_001165283.1:p.Pro140=