Canonical Allele Identifier: CA6884115
Community Standard Title: NM_025215.6(PUS1):c.426C>T (p.Cys142=)
Gene: PUS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131932297C>T , CM000674.2:g.131932297C>T GRCh38
NC_000012.11:g.132416842C>T , CM000674.1:g.132416842C>T GRCh37
NC_000012.10:g.130982795C>T NCBI36
NG_013039.1:g.8098C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025215.6:c.426C>T MANE Select NP_079491.2:p.Cys142=
ENST00000376649.8:c.426C>T MANE Select ENSP00000365837.3:p.Cys142=
NM_001002019.2:c.342C>T NP_001002019.1:p.Cys114=
NM_001002019.3:c.342C>T NP_001002019.1:p.Cys114=
NM_001002020.2:c.342C>T NP_001002020.1:p.Cys114=
NM_001002020.3:c.342C>T NP_001002020.1:p.Cys114=
NM_025215.5:c.426C>T NP_079491.2:p.Cys142=
ENST00000322060.9:c.342C>T ENSP00000324726.5:p.Cys114=
ENST00000376649.7:c.426C>T ENSP00000365837.3:p.Cys142=
ENST00000443358.6:c.342C>T ENSP00000392451.2:p.Cys114=
ENST00000456665.6:c.342C>T ENSP00000409705.2:p.Cys114=
ENST00000535067.5:c.342C>T ENSP00000443969.1:p.Cys114=
ENST00000537484.1:c.342C>T ENSP00000440179.1:p.Cys114=
ENST00000538037.5:c.342C>T ENSP00000440326.2:p.Cys114=
ENST00000542167.2:c.267C>T ENSP00000438948.1:p.Cys89=
ENST00000544213.5:c.426C>T ENSP00000445819.1:p.Cys142=
ENST00000544662.1:n.453C>T
XM_011538768.1:c.27C>T XP_011537070.1:p.Cys9=
XM_011538768.3:c.27C>T XP_011537070.1:p.Cys9=
XM_011538769.1:c.426C>T XP_011537071.1:p.Cys142=
XM_011538769.2:c.426C>T XP_011537071.1:p.Cys142=
XR_001748872.1:n.881C>T
XR_944737.1:n.881C>T