Canonical Allele Identifier: CA396120341
Community Standard Title: NM_001080432.3(FTO):c.956C>G (p.Ser319Cys)
Gene: FTO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.53873846C>G , CM000678.2:g.53873846C>G GRCh38
NC_000016.9:g.53907758C>G , CM000678.1:g.53907758C>G GRCh37
NC_000016.8:g.52465259C>G NCBI36
NG_012969.1:g.174884C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001080432.3:c.956C>G MANE Select NP_001073901.1:p.Ser319Cys
ENST00000471389.6:c.956C>G MANE Select ENSP00000418823.1:p.Ser319Cys
NM_001080432.2:c.956C>G NP_001073901.1:p.Ser319Cys
NM_001363891.1:c.986C>G NP_001350820.1:p.Ser329Cys
NM_001363894.1:c.956C>G NP_001350823.1:p.Ser319Cys
NM_001363896.1:c.956C>G NP_001350825.1:p.Ser319Cys
NM_001363897.1:c.878C>G NP_001350826.1:p.Ser293Cys
NM_001363898.1:c.986C>G NP_001350827.1:p.Ser329Cys
NM_001363899.1:c.842C>G NP_001350828.1:p.Ser281Cys
NM_001363900.1:c.956C>G NP_001350829.1:p.Ser319Cys
NM_001363901.1:c.812C>G NP_001350830.1:p.Ser271Cys
NM_001363903.1:c.956C>G NP_001350832.1:p.Ser319Cys
NM_001363905.1:c.443C>G NP_001350834.1:p.Ser148Cys
NM_001363988.1:c.956C>G NP_001350917.1:p.Ser319Cys
NR_156761.1:n.489+29548C>G
ENST00000464071.1:c.*115C>G ENSP00000418424.1:n.*115C>G
ENST00000471389.5:c.956C>G ENSP00000418823.1:p.Ser319Cys
ENST00000563011.2:c.336C>G
ENST00000636030.1:n.983C>G
ENST00000636218.1:c.956C>G ENSP00000489641.1:p.Ser319Cys
ENST00000636491.1:c.938C>G ENSP00000490047.1:p.Ser313Cys
ENST00000636992.1:c.956C>G ENSP00000489886.1:p.Ser319Cys
ENST00000637001.1:c.956C>G ENSP00000489936.1:p.Ser319Cys
ENST00000637562.1:c.956C>G ENSP00000490426.1:p.Ser319Cys
ENST00000637845.1:c.956C>G ENSP00000489638.1:p.Ser319Cys
ENST00000637969.1:c.956C>G ENSP00000490516.1:p.Ser319Cys
XM_011523313.1:c.986C>G XP_011521615.1:p.Ser329Cys
XM_011523314.1:c.986C>G XP_011521616.1:p.Ser329Cys
XM_011523314.3:c.986C>G XP_011521616.1:p.Ser329Cys
XM_011523315.1:c.986C>G XP_011521617.1:p.Ser329Cys
XM_011523315.3:c.986C>G XP_011521617.1:p.Ser329Cys
XM_011523316.1:c.986C>G XP_011521618.1:p.Ser329Cys
XM_011523316.3:c.986C>G XP_011521618.1:p.Ser329Cys
XM_017023654.2:c.986C>G XP_016879143.1:p.Ser329Cys
XM_017023655.2:c.956C>G XP_016879144.1:p.Ser319Cys
XM_017023656.2:c.956C>G XP_016879145.1:p.Ser319Cys
XM_017023657.2:c.956C>G XP_016879146.1:p.Ser319Cys
XM_024450437.1:c.956C>G XP_024306205.1:p.Ser319Cys
XR_002957840.1:n.1233C>G