Canonical Allele Identifier: CA387298785
Gene: PUS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131941349A>T , CM000674.2:g.131941349A>T GRCh38
NC_000012.11:g.132425894A>T , CM000674.1:g.132425894A>T GRCh37
NC_000012.10:g.130991847A>T NCBI36
NG_013039.1:g.17150A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376649.8:c.602A>T MANE Select ENSP00000365837.3:p.Tyr201Phe
ENST00000322060.9:c.518A>T ENSP00000324726.5:p.Tyr173Phe
ENST00000376649.7:c.602A>T ENSP00000365837.3:p.Tyr201Phe
ENST00000443358.6:c.518A>T ENSP00000392451.2:p.Tyr173Phe
ENST00000535067.5:c.358-2190A>T ENSP00000443969.1:n.358-2190A>T
ENST00000537484.1:c.527A>T ENSP00000440179.1:p.Tyr176Phe
ENST00000542167.2:c.443A>T ENSP00000438948.1:p.Tyr148Phe
ENST00000543754.1:n.423A>T
NM_001002019.2:c.518A>T NP_001002019.1:p.Tyr173Phe
NM_001002020.2:c.518A>T NP_001002020.1:p.Tyr173Phe
NM_025215.5:c.602A>T NP_079491.2:p.Tyr201Phe
XM_011538768.1:c.203A>T XP_011537070.1:p.Tyr68Phe
XM_011538768.3:c.203A>T XP_011537070.1:p.Tyr68Phe
XR_001748872.1:n.1057A>T
NM_001002019.3:c.518A>T NP_001002019.1:p.Tyr173Phe
NM_001002020.3:c.518A>T NP_001002020.1:p.Tyr173Phe
NM_025215.6:c.602A>T MANE Select NP_079491.2:p.Tyr201Phe