Canonical Allele Identifier: CA387299030
Gene: PUS1 HGNC NCBI

Linked Data

dbSNP Id: rs1157115342

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131941466A>G , CM000674.2:g.131941466A>G GRCh38
NC_000012.11:g.132426011A>G , CM000674.1:g.132426011A>G GRCh37
NC_000012.10:g.130991964A>G NCBI36
NG_013039.1:g.17267A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376649.8:c.719A>G MANE Select ENSP00000365837.3:p.Lys240Arg
ENST00000322060.9:c.635A>G ENSP00000324726.5:p.Lys212Arg
ENST00000376649.7:c.719A>G ENSP00000365837.3:p.Lys240Arg
ENST00000443358.6:c.635A>G ENSP00000392451.2:p.Lys212Arg
ENST00000535067.5:c.358-2073A>G ENSP00000443969.1:n.358-2073A>G
ENST00000542167.2:c.560A>G ENSP00000438948.1:p.Lys187Arg
ENST00000543754.1:n.540A>G
NM_001002019.2:c.635A>G NP_001002019.1:p.Lys212Arg
NM_001002020.2:c.635A>G NP_001002020.1:p.Lys212Arg
NM_025215.5:c.719A>G NP_079491.2:p.Lys240Arg
XM_011538768.1:c.320A>G XP_011537070.1:p.Lys107Arg
XM_011538768.3:c.320A>G XP_011537070.1:p.Lys107Arg
XR_001748872.1:n.1174A>G
NM_001002019.3:c.635A>G NP_001002019.1:p.Lys212Arg
NM_001002020.3:c.635A>G NP_001002020.1:p.Lys212Arg
NM_025215.6:c.719A>G MANE Select NP_079491.2:p.Lys240Arg