Canonical Allele Identifier: CA342722302
Gene: GBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155238233G>T , CM000663.2:g.155238233G>T GRCh38
NC_000001.10:g.155208024G>T , CM000663.1:g.155208024G>T GRCh37
NC_000001.9:g.153474648G>T NCBI36
NG_009783.1:g.11465C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368373.8:c.662C>A MANE Select ENSP00000357357.3:p.Pro221His
ENST00000327247.9:c.662C>A ENSP00000314508.5:p.Pro221His
ENST00000368373.7:c.662C>A ENSP00000357357.3:p.Pro221His
ENST00000427500.7:c.515C>A ENSP00000402577.2:p.Pro172His
ENST00000428024.3:c.401C>A ENSP00000397986.2:p.Pro134His
ENST00000460156.1:n.449C>A
ENST00000484489.5:n.339+1740C>A
ENST00000491081.5:n.267C>A
ENST00000493842.5:n.1000C>A
ENST00000497670.5:n.285C>A
NM_000157.3:c.662C>A NP_000148.2:p.Pro221His
NM_001005741.2:c.662C>A NP_001005741.1:p.Pro221His
NM_001005742.2:c.662C>A NP_001005742.1:p.Pro221His
NM_001171811.1:c.401C>A NP_001165282.1:p.Pro134His
NM_001171812.1:c.515C>A NP_001165283.1:p.Pro172His
XM_006711270.1:c.662C>A XP_006711333.1:p.Pro221His
XM_011509407.1:c.662C>A XP_011507709.1:p.Pro221His
NM_000157.4:c.662C>A MANE Select NP_000148.2:p.Pro221His
NM_001005741.3:c.662C>A NP_001005741.1:p.Pro221His
NM_001005742.3:c.662C>A NP_001005742.1:p.Pro221His
NM_001171811.2:c.401C>A NP_001165282.1:p.Pro134His
NM_001171812.2:c.515C>A NP_001165283.1:p.Pro172His