Canonical Allele Identifier: CA6884196
Gene: PUS1 HGNC NCBI

Linked Data

dbSNP Id: rs758761710

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131941325A>G , CM000674.2:g.131941325A>G GRCh38
NC_000012.11:g.132425870A>G , CM000674.1:g.132425870A>G GRCh37
NC_000012.10:g.130991823A>G NCBI36
NG_013039.1:g.17126A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376649.8:c.578A>G MANE Select ENSP00000365837.3:p.Lys193Arg
ENST00000322060.9:c.494A>G ENSP00000324726.5:p.Lys165Arg
ENST00000376649.7:c.578A>G ENSP00000365837.3:p.Lys193Arg
ENST00000443358.6:c.494A>G ENSP00000392451.2:p.Lys165Arg
ENST00000535067.5:c.358-2214A>G ENSP00000443969.1:n.358-2214A>G
ENST00000537484.1:c.503A>G ENSP00000440179.1:p.Lys168Arg
ENST00000542167.2:c.419A>G ENSP00000438948.1:p.Lys140Arg
ENST00000543754.1:n.399A>G
NM_001002019.2:c.494A>G NP_001002019.1:p.Lys165Arg
NM_001002020.2:c.494A>G NP_001002020.1:p.Lys165Arg
NM_025215.5:c.578A>G NP_079491.2:p.Lys193Arg
XM_011538768.1:c.179A>G XP_011537070.1:p.Lys60Arg
XM_011538768.3:c.179A>G XP_011537070.1:p.Lys60Arg
XR_001748872.1:n.1033A>G
NM_001002019.3:c.494A>G NP_001002019.1:p.Lys165Arg
NM_001002020.3:c.494A>G NP_001002020.1:p.Lys165Arg
NM_025215.6:c.578A>G MANE Select NP_079491.2:p.Lys193Arg