Canonical Allele Identifier: CA146984
Community Standard Title: NM_000157.4(GBA1):c.605G>A (p.Arg202Gln)
Gene: GBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155238290C>T , CM000663.2:g.155238290C>T GRCh38
NC_000001.10:g.155208081C>T , CM000663.1:g.155208081C>T GRCh37
NC_000001.9:g.153474705C>T NCBI36
NG_009783.1:g.11408G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000157.4:c.605G>A MANE Select NP_000148.2:p.Arg202Gln
ENST00000368373.8:c.605G>A MANE Select ENSP00000357357.3:p.Arg202Gln
NM_000157.3:c.605G>A NP_000148.2:p.Arg202Gln
NM_001005741.2:c.605G>A NP_001005741.1:p.Arg202Gln
NM_001005741.3:c.605G>A NP_001005741.1:p.Arg202Gln
NM_001005742.2:c.605G>A NP_001005742.1:p.Arg202Gln
NM_001005742.3:c.605G>A NP_001005742.1:p.Arg202Gln
NM_001171811.1:c.344G>A NP_001165282.1:p.Arg115Gln
NM_001171811.2:c.344G>A NP_001165282.1:p.Arg115Gln
NM_001171812.1:c.458G>A NP_001165283.1:p.Arg153Gln
NM_001171812.2:c.458G>A NP_001165283.1:p.Arg153Gln
ENST00000327247.9:c.605G>A ENSP00000314508.5:p.Arg202Gln
ENST00000368373.7:c.605G>A ENSP00000357357.3:p.Arg202Gln
ENST00000427500.7:c.458G>A ENSP00000402577.2:p.Arg153Gln
ENST00000428024.3:c.344G>A ENSP00000397986.2:p.Arg115Gln
ENST00000460156.1:n.392G>A
ENST00000484489.5:n.339+1683G>A
ENST00000491081.5:n.210G>A
ENST00000493842.5:n.943G>A
ENST00000497670.5:n.228G>A
XM_006711270.1:c.605G>A XP_006711333.1:p.Arg202Gln
XM_011509407.1:c.605G>A XP_011507709.1:p.Arg202Gln