Canonical Allele Identifier: CA30895561

Gene: GBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155238234G>T , CM000663.2:g.155238234G>T	GRCh38
NC_000001.10:g.155208025G>T , CM000663.1:g.155208025G>T	GRCh37
NC_000001.9:g.153474649G>T	NCBI36
NG_009783.1:g.11464C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000157.4:c.661C>A MANE Select	NP_000148.2:p.Pro221Thr
ENST00000368373.8:c.661C>A MANE Select	ENSP00000357357.3:p.Pro221Thr
NM_000157.3:c.661C>A	NP_000148.2:p.Pro221Thr
NM_001005741.2:c.661C>A	NP_001005741.1:p.Pro221Thr
NM_001005741.3:c.661C>A	NP_001005741.1:p.Pro221Thr
NM_001005742.2:c.661C>A	NP_001005742.1:p.Pro221Thr
NM_001005742.3:c.661C>A	NP_001005742.1:p.Pro221Thr
NM_001171811.1:c.400C>A	NP_001165282.1:p.Pro134Thr
NM_001171811.2:c.400C>A	NP_001165282.1:p.Pro134Thr
NM_001171812.1:c.514C>A	NP_001165283.1:p.Pro172Thr
NM_001171812.2:c.514C>A	NP_001165283.1:p.Pro172Thr
ENST00000327247.9:c.661C>A	ENSP00000314508.5:p.Pro221Thr
ENST00000368373.7:c.661C>A	ENSP00000357357.3:p.Pro221Thr
ENST00000427500.7:c.514C>A	ENSP00000402577.2:p.Pro172Thr
ENST00000428024.3:c.400C>A	ENSP00000397986.2:p.Pro134Thr
ENST00000460156.1:n.448C>A
ENST00000484489.5:n.339+1739C>A
ENST00000491081.5:n.266C>A
ENST00000493842.5:n.999C>A
ENST00000497670.5:n.284C>A
XM_006711270.1:c.661C>A	XP_006711333.1:p.Pro221Thr
XM_011509407.1:c.661C>A	XP_011507709.1:p.Pro221Thr