Canonical Allele Identifier: CA2223353843
Gene: FTO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.53767511_53767512delinsAT , CM000678.2:g.53767511_53767512delinsAT GRCh38
NC_000016.9:g.53801423_53801424delinsAT , CM000678.1:g.53801423_53801424delinsAT GRCh37
NC_000016.8:g.52358924_52358925delinsAT NCBI36
NG_012969.1:g.68549_68550delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000471389.6:c.46-42629_46-42628delinsAT MANE Select ENSP00000418823.1:n.46-42629_46-42628delinsAT
ENST00000636030.1:n.73-42629_73-42628delinsAT
ENST00000636218.1:c.46-42629_46-42628delinsAT ENSP00000489641.1:n.46-42629_46-42628delinsAT
ENST00000636491.1:c.28-42629_28-42628delinsAT ENSP00000490047.1:n.28-42629_28-42628delinsAT
ENST00000636992.1:c.46-42629_46-42628delinsAT ENSP00000489886.1:n.46-42629_46-42628delinsAT
ENST00000637001.1:c.46-42629_46-42628delinsAT ENSP00000489936.1:n.46-42629_46-42628delinsAT
ENST00000637562.1:c.46-42629_46-42628delinsAT ENSP00000490426.1:n.46-42629_46-42628delinsAT
ENST00000637845.1:c.46-42629_46-42628delinsAT ENSP00000489638.1:n.46-42629_46-42628delinsAT
ENST00000637969.1:c.46-42629_46-42628delinsAT ENSP00000490516.1:n.46-42629_46-42628delinsAT
ENST00000640179.1:c.46-42629_46-42628delinsAT ENSP00000490980.1:n.46-42629_46-42628delinsAT
ENST00000464071.1:c.46-42629_46-42628delinsAT ENSP00000418424.1:n.46-42629_46-42628delinsAT
ENST00000471389.5:c.46-42629_46-42628delinsAT ENSP00000418823.1:n.46-42629_46-42628delinsAT
ENST00000570395.1:n.193+3231_193+3232delinsAT
NM_001080432.2:c.46-42629_46-42628delinsAT NP_001073901.1:n.46-42629_46-42628delinsAT
XM_011523313.1:c.46-42629_46-42628delinsAT XP_011521615.1:n.46-42629_46-42628delinsAT
XM_011523314.1:c.46-42629_46-42628delinsAT XP_011521616.1:n.46-42629_46-42628delinsAT
XM_011523315.1:c.46-42629_46-42628delinsAT XP_011521617.1:n.46-42629_46-42628delinsAT
XM_011523316.1:c.46-42629_46-42628delinsAT XP_011521618.1:n.46-42629_46-42628delinsAT
NM_001363891.1:c.46-42629_46-42628delinsAT NP_001350820.1:n.46-42629_46-42628delinsAT
NM_001363894.1:c.46-42629_46-42628delinsAT NP_001350823.1:n.46-42629_46-42628delinsAT
NM_001363896.1:c.46-42629_46-42628delinsAT NP_001350825.1:n.46-42629_46-42628delinsAT
NM_001363897.1:c.46-58353_46-58352delinsAT NP_001350826.1:n.46-58353_46-58352delinsAT
NM_001363898.1:c.46-42629_46-42628delinsAT NP_001350827.1:n.46-42629_46-42628delinsAT
NM_001363899.1:c.46-42629_46-42628delinsAT NP_001350828.1:n.46-42629_46-42628delinsAT
NM_001363900.1:c.46-42629_46-42628delinsAT NP_001350829.1:n.46-42629_46-42628delinsAT
NM_001363901.1:c.46-42629_46-42628delinsAT NP_001350830.1:n.46-42629_46-42628delinsAT
NM_001363903.1:c.46-42629_46-42628delinsAT NP_001350832.1:n.46-42629_46-42628delinsAT
NM_001363905.1:c.-647-42629_-647-42628delinsAT NP_001350834.1:n.-647-42629_-647-42628delinsAT
NM_001363988.1:c.46-42629_46-42628delinsAT NP_001350917.1:n.46-42629_46-42628delinsAT
NR_156761.1:n.268-42629_268-42628delinsAT
XM_011523314.3:c.46-42629_46-42628delinsAT XP_011521616.1:n.46-42629_46-42628delinsAT
XM_011523315.3:c.46-42629_46-42628delinsAT XP_011521617.1:n.46-42629_46-42628delinsAT
XM_011523316.3:c.46-42629_46-42628delinsAT XP_011521618.1:n.46-42629_46-42628delinsAT
XM_017023654.2:c.46-42629_46-42628delinsAT XP_016879143.1:n.46-42629_46-42628delinsAT
XM_017023655.2:c.46-42629_46-42628delinsAT XP_016879144.1:n.46-42629_46-42628delinsAT
XM_017023656.2:c.46-42629_46-42628delinsAT XP_016879145.1:n.46-42629_46-42628delinsAT
XM_017023657.2:c.46-42629_46-42628delinsAT XP_016879146.1:n.46-42629_46-42628delinsAT
XM_017023658.2:c.46-42629_46-42628delinsAT XP_016879147.1:n.46-42629_46-42628delinsAT
XM_024450437.1:c.46-42629_46-42628delinsAT XP_024306205.1:n.46-42629_46-42628delinsAT
XR_002957840.1:n.89-42629_89-42628delinsAT
NM_001080432.3:c.46-42629_46-42628delinsAT MANE Select NP_001073901.1:n.46-42629_46-42628delinsAT