Canonical Allele Identifier: CA387298936
Gene: PUS1 HGNC NCBI

Linked Data

dbSNP Id: rs1891059140

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131941421G>A , CM000674.2:g.131941421G>A GRCh38
NC_000012.11:g.132425966G>A , CM000674.1:g.132425966G>A GRCh37
NC_000012.10:g.130991919G>A NCBI36
NG_013039.1:g.17222G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376649.8:c.674G>A MANE Select ENSP00000365837.3:p.Ser225Asn
ENST00000322060.9:c.590G>A ENSP00000324726.5:p.Ser197Asn
ENST00000376649.7:c.674G>A ENSP00000365837.3:p.Ser225Asn
ENST00000443358.6:c.590G>A ENSP00000392451.2:p.Ser197Asn
ENST00000535067.5:c.358-2118G>A ENSP00000443969.1:n.358-2118G>A
ENST00000537484.1:c.599G>A ENSP00000440179.1:p.Ser200Asn
ENST00000542167.2:c.515G>A ENSP00000438948.1:p.Ser172Asn
ENST00000543754.1:n.495G>A
NM_001002019.2:c.590G>A NP_001002019.1:p.Ser197Asn
NM_001002020.2:c.590G>A NP_001002020.1:p.Ser197Asn
NM_025215.5:c.674G>A NP_079491.2:p.Ser225Asn
XM_011538768.1:c.275G>A XP_011537070.1:p.Ser92Asn
XM_011538768.3:c.275G>A XP_011537070.1:p.Ser92Asn
XR_001748872.1:n.1129G>A
NM_001002019.3:c.590G>A NP_001002019.1:p.Ser197Asn
NM_001002020.3:c.590G>A NP_001002020.1:p.Ser197Asn
NM_025215.6:c.674G>A MANE Select NP_079491.2:p.Ser225Asn