Canonical Allele Identifier: CA387298796
Gene: PUS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131941354T>C , CM000674.2:g.131941354T>C GRCh38
NC_000012.11:g.132425899T>C , CM000674.1:g.132425899T>C GRCh37
NC_000012.10:g.130991852T>C NCBI36
NG_013039.1:g.17155T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376649.8:c.607T>C MANE Select ENSP00000365837.3:p.Tyr203His
ENST00000322060.9:c.523T>C ENSP00000324726.5:p.Tyr175His
ENST00000376649.7:c.607T>C ENSP00000365837.3:p.Tyr203His
ENST00000443358.6:c.523T>C ENSP00000392451.2:p.Tyr175His
ENST00000535067.5:c.358-2185T>C ENSP00000443969.1:n.358-2185T>C
ENST00000537484.1:c.532T>C ENSP00000440179.1:p.Tyr178His
ENST00000542167.2:c.448T>C ENSP00000438948.1:p.Tyr150His
ENST00000543754.1:n.428T>C
NM_001002019.2:c.523T>C NP_001002019.1:p.Tyr175His
NM_001002020.2:c.523T>C NP_001002020.1:p.Tyr175His
NM_025215.5:c.607T>C NP_079491.2:p.Tyr203His
XM_011538768.1:c.208T>C XP_011537070.1:p.Tyr70His
XM_011538768.3:c.208T>C XP_011537070.1:p.Tyr70His
XR_001748872.1:n.1062T>C
NM_001002019.3:c.523T>C NP_001002019.1:p.Tyr175His
NM_001002020.3:c.523T>C NP_001002020.1:p.Tyr175His
NM_025215.6:c.607T>C MANE Select NP_079491.2:p.Tyr203His