Canonical Allele Identifier: CA387299004
Gene: PUS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131941454T>A , CM000674.2:g.131941454T>A GRCh38
NC_000012.11:g.132425999T>A , CM000674.1:g.132425999T>A GRCh37
NC_000012.10:g.130991952T>A NCBI36
NG_013039.1:g.17255T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376649.8:c.707T>A MANE Select ENSP00000365837.3:p.Leu236Gln
ENST00000322060.9:c.623T>A ENSP00000324726.5:p.Leu208Gln
ENST00000376649.7:c.707T>A ENSP00000365837.3:p.Leu236Gln
ENST00000443358.6:c.623T>A ENSP00000392451.2:p.Leu208Gln
ENST00000535067.5:c.358-2085T>A ENSP00000443969.1:n.358-2085T>A
ENST00000542167.2:c.548T>A ENSP00000438948.1:p.Leu183Gln
ENST00000543754.1:n.528T>A
NM_001002019.2:c.623T>A NP_001002019.1:p.Leu208Gln
NM_001002020.2:c.623T>A NP_001002020.1:p.Leu208Gln
NM_025215.5:c.707T>A NP_079491.2:p.Leu236Gln
XM_011538768.1:c.308T>A XP_011537070.1:p.Leu103Gln
XM_011538768.3:c.308T>A XP_011537070.1:p.Leu103Gln
XR_001748872.1:n.1162T>A
NM_001002019.3:c.623T>A NP_001002019.1:p.Leu208Gln
NM_001002020.3:c.623T>A NP_001002020.1:p.Leu208Gln
NM_025215.6:c.707T>A MANE Select NP_079491.2:p.Leu236Gln