Canonical Allele Identifier: CA2842197518

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238683C>A , CM000663.2:g.155238683C>A	GRCh38
NC_000001.10:g.155208474C>A , CM000663.1:g.155208474C>A	GRCh37
NC_000001.9:g.153475098C>A	NCBI36
NG_009783.1:g.11015G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368373.8:c.455-33G>T MANE Select	ENSP00000357357.3:n.455-33G>T
ENST00000327247.9:c.455-33G>T	ENSP00000314508.5:n.455-33G>T
ENST00000368373.7:c.455-33G>T	ENSP00000357357.3:n.455-33G>T
ENST00000427500.7:c.308-33G>T	ENSP00000402577.2:n.308-33G>T
ENST00000428024.3:c.194-33G>T	ENSP00000397986.2:n.194-33G>T
ENST00000460156.1:n.209G>T
ENST00000473570.5:n.776-33G>T
ENST00000484489.5:n.339+1290G>T
ENST00000491081.5:n.27G>T
ENST00000493842.5:n.793-33G>T
ENST00000497670.5:n.78-33G>T
NM_000157.3:c.455-33G>T	NP_000148.2:n.455-33G>T
NM_001005741.2:c.455-33G>T	NP_001005741.1:n.455-33G>T
NM_001005742.2:c.455-33G>T	NP_001005742.1:n.455-33G>T
NM_001171811.1:c.194-33G>T	NP_001165282.1:n.194-33G>T
NM_001171812.1:c.308-33G>T	NP_001165283.1:n.308-33G>T
XM_006711270.1:c.455-33G>T	XP_006711333.1:n.455-33G>T
XM_011509407.1:c.455-33G>T	XP_011507709.1:n.455-33G>T
NM_000157.4:c.455-33G>T MANE Select	NP_000148.2:n.455-33G>T
NM_001005741.3:c.455-33G>T	NP_001005741.1:n.455-33G>T
NM_001005742.3:c.455-33G>T	NP_001005742.1:n.455-33G>T
NM_001171811.2:c.194-33G>T	NP_001165282.1:n.194-33G>T
NM_001171812.2:c.308-33G>T	NP_001165283.1:n.308-33G>T