Canonical Allele Identifier: CA387298803
Gene: PUS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131941356C>G , CM000674.2:g.131941356C>G GRCh38
NC_000012.11:g.132425901C>G , CM000674.1:g.132425901C>G GRCh37
NC_000012.10:g.130991854C>G NCBI36
NG_013039.1:g.17157C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376649.8:c.609C>G MANE Select ENSP00000365837.3:p.Tyr203Ter
ENST00000322060.9:c.525C>G ENSP00000324726.5:p.Tyr175Ter
ENST00000376649.7:c.609C>G ENSP00000365837.3:p.Tyr203Ter
ENST00000443358.6:c.525C>G ENSP00000392451.2:p.Tyr175Ter
ENST00000535067.5:c.358-2183C>G ENSP00000443969.1:n.358-2183C>G
ENST00000537484.1:c.534C>G ENSP00000440179.1:p.Tyr178Ter
ENST00000542167.2:c.450C>G ENSP00000438948.1:p.Tyr150Ter
ENST00000543754.1:n.430C>G
NM_001002019.2:c.525C>G NP_001002019.1:p.Tyr175Ter
NM_001002020.2:c.525C>G NP_001002020.1:p.Tyr175Ter
NM_025215.5:c.609C>G NP_079491.2:p.Tyr203Ter
XM_011538768.1:c.210C>G XP_011537070.1:p.Tyr70Ter
XM_011538768.3:c.210C>G XP_011537070.1:p.Tyr70Ter
XR_001748872.1:n.1064C>G
NM_001002019.3:c.525C>G NP_001002019.1:p.Tyr175Ter
NM_001002020.3:c.525C>G NP_001002020.1:p.Tyr175Ter
NM_025215.6:c.609C>G MANE Select NP_079491.2:p.Tyr203Ter