Canonical Allele Identifier: CA421020549

Gene: GBA1

Linked Data

• MyVariant Identifiers: chr1:g.155206084C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155236293C>A , CM000663.2:g.155236293C>A	GRCh38
NC_000001.10:g.155206084C>A , CM000663.1:g.155206084C>A	GRCh37
NC_000001.9:g.153472708C>A	NCBI36
NG_009783.1:g.13405G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.1176G>T MANE Select	ENSP00000357357.3:p.Arg392=
ENST00000327247.9:c.1176G>T	ENSP00000314508.5:p.Arg392=
ENST00000368373.7:c.1176G>T	ENSP00000357357.3:p.Arg392=
ENST00000427500.7:c.1029G>T	ENSP00000402577.2:p.Arg343=
ENST00000428024.3:c.915G>T	ENSP00000397986.2:p.Arg305=
ENST00000478472.1:n.167G>T
ENST00000484489.5:n.340-5G>T
ENST00000491081.5:n.781G>T
NM_000157.3:c.1176G>T	NP_000148.2:p.Arg392=
NM_001005741.2:c.1176G>T	NP_001005741.1:p.Arg392=
NM_001005742.2:c.1176G>T	NP_001005742.1:p.Arg392=
NM_001171811.1:c.915G>T	NP_001165282.1:p.Arg305=
NM_001171812.1:c.1029G>T	NP_001165283.1:p.Arg343=
XM_006711270.1:c.1176G>T	XP_006711333.1:p.Arg392=
XM_011509407.1:c.1176G>T	XP_011507709.1:p.Arg392=
NM_000157.4:c.1176G>T MANE Select	NP_000148.2:p.Arg392=
NM_001005741.3:c.1176G>T	NP_001005741.1:p.Arg392=
NM_001005742.3:c.1176G>T	NP_001005742.1:p.Arg392=
NM_001171811.2:c.915G>T	NP_001165282.1:p.Arg305=
NM_001171812.2:c.1029G>T	NP_001165283.1:p.Arg343=