Canonical Allele Identifier: CA2223441207
Gene: FTO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.53994042_53994046delinsGTTAT , CM000678.2:g.53994042_53994046delinsGTTAT GRCh38
NC_000016.9:g.54027954_54027958delinsGTTAT , CM000678.1:g.54027954_54027958delinsGTTAT GRCh37
NC_000016.8:g.52585455_52585459delinsGTTAT NCBI36
NG_012969.1:g.295080_295084delinsGTTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000471389.6:c.1364+59933_1364+59937delinsGTTAT MANE Select ENSP00000418823.1:n.1364+59933_1364+59937delinsGTTAT
ENST00000563011.2:c.745-45303_745-45299delinsGTTAT
ENST00000612285.2:c.389+59933_389+59937delinsGTTAT ENSP00000490300.1:n.389+59933_389+59937delinsGTTAT
ENST00000635892.1:n.214+59933_214+59937delinsGTTAT
ENST00000636491.1:c.1347-14386_1347-14382delinsGTTAT ENSP00000490047.1:n.1347-14386_1347-14382delinsGTTAT
ENST00000636992.1:c.1240-19336_1240-19332delinsGTTAT ENSP00000489886.1:n.1240-19336_1240-19332delinsGTTAT
ENST00000637562.1:c.1364+59933_1364+59937delinsGTTAT ENSP00000490426.1:n.1364+59933_1364+59937delinsGTTAT
ENST00000637845.1:c.1364+59933_1364+59937delinsGTTAT ENSP00000489638.1:n.1364+59933_1364+59937delinsGTTAT
ENST00000637969.1:c.1364+59933_1364+59937delinsGTTAT ENSP00000490516.1:n.1364+59933_1364+59937delinsGTTAT
ENST00000268349.7:c.97+9088_97+9092delinsGTTAT ENSP00000268349.7:n.97+9088_97+9092delinsGTTAT
ENST00000431610.6:c.167+59933_167+59937delinsGTTAT ENSP00000415636.2:n.167+59933_167+59937delinsGTTAT
ENST00000460382.5:c.167+59933_167+59937delinsGTTAT ENSP00000417422.1:n.167+59933_167+59937delinsGTTAT
ENST00000463855.1:c.230+59933_230+59937delinsGTTAT ENSP00000417843.1:n.230+59933_230+59937delinsGTTAT
ENST00000464071.1:c.*523+59933_*523+59937delinsGTTAT ENSP00000418424.1:n.*523+59933_*523+59937delinsGTTAT
ENST00000471389.5:c.1364+59933_1364+59937delinsGTTAT ENSP00000418823.1:n.1364+59933_1364+59937delinsGTTAT
NM_001080432.2:c.1364+59933_1364+59937delinsGTTAT NP_001073901.1:n.1364+59933_1364+59937delinsGTTAT
XM_011523313.1:c.1394+59933_1394+59937delinsGTTAT XP_011521615.1:n.1394+59933_1394+59937delinsGTTAT
XM_011523316.1:c.1395-14386_1395-14382delinsGTTAT XP_011521618.1:n.1395-14386_1395-14382delinsGTTAT
NM_001363891.1:c.1394+59933_1394+59937delinsGTTAT NP_001350820.1:n.1394+59933_1394+59937delinsGTTAT
NM_001363894.1:c.1427+59933_1427+59937delinsGTTAT NP_001350823.1:n.1427+59933_1427+59937delinsGTTAT
NM_001363896.1:c.1346+37253_1346+37257delinsGTTAT NP_001350825.1:n.1346+37253_1346+37257delinsGTTAT
NM_001363897.1:c.1286+59933_1286+59937delinsGTTAT NP_001350826.1:n.1286+59933_1286+59937delinsGTTAT
NM_001363898.1:c.1250+59933_1250+59937delinsGTTAT NP_001350827.1:n.1250+59933_1250+59937delinsGTTAT
NM_001363899.1:c.1250+59933_1250+59937delinsGTTAT NP_001350828.1:n.1250+59933_1250+59937delinsGTTAT
NM_001363900.1:c.1220+59933_1220+59937delinsGTTAT NP_001350829.1:n.1220+59933_1220+59937delinsGTTAT
NM_001363901.1:c.1220+59933_1220+59937delinsGTTAT NP_001350830.1:n.1220+59933_1220+59937delinsGTTAT
NM_001363903.1:c.1239+105091_1239+105095delinsGTTAT NP_001350832.1:n.1239+105091_1239+105095delinsGTTAT
NM_001363905.1:c.851+59933_851+59937delinsGTTAT NP_001350834.1:n.851+59933_851+59937delinsGTTAT
NM_001363988.1:c.*22+37253_*22+37257delinsGTTAT NP_001350917.1:n.*22+37253_*22+37257delinsGTTAT
NR_156761.1:n.614+59933_614+59937delinsGTTAT
XM_011523316.3:c.1395-14386_1395-14382delinsGTTAT XP_011521618.1:n.1395-14386_1395-14382delinsGTTAT
XM_024450437.1:c.1365-14386_1365-14382delinsGTTAT XP_024306205.1:n.1365-14386_1365-14382delinsGTTAT
NM_001080432.3:c.1364+59933_1364+59937delinsGTTAT MANE Select NP_001073901.1:n.1364+59933_1364+59937delinsGTTAT