Canonical Allele Identifier: CA2223441195
Gene: FTO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.53994017_53994018delinsAT , CM000678.2:g.53994017_53994018delinsAT GRCh38
NC_000016.9:g.54027929_54027930delinsAT , CM000678.1:g.54027929_54027930delinsAT GRCh37
NC_000016.8:g.52585430_52585431delinsAT NCBI36
NG_012969.1:g.295055_295056delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000471389.6:c.1364+59908_1364+59909delinsAT MANE Select ENSP00000418823.1:n.1364+59908_1364+59909...
ENST00000563011.2:c.745-45328_745-45327delinsAT
ENST00000612285.2:c.389+59908_389+59909delinsAT ENSP00000490300.1:n.389+59908_389+59909de...
ENST00000635892.1:n.214+59908_214+59909delinsAT
ENST00000636491.1:c.1347-14411_1347-14410delinsAT ENSP00000490047.1:n.1347-14411_1347-14410...
ENST00000636992.1:c.1240-19361_1240-19360delinsAT ENSP00000489886.1:n.1240-19361_1240-19360...
ENST00000637562.1:c.1364+59908_1364+59909delinsAT ENSP00000490426.1:n.1364+59908_1364+59909...
ENST00000637845.1:c.1364+59908_1364+59909delinsAT ENSP00000489638.1:n.1364+59908_1364+59909...
ENST00000637969.1:c.1364+59908_1364+59909delinsAT ENSP00000490516.1:n.1364+59908_1364+59909...
ENST00000268349.7:c.97+9063_97+9064delinsAT ENSP00000268349.7:n.97+9063_97+9064delins...
ENST00000431610.6:c.167+59908_167+59909delinsAT ENSP00000415636.2:n.167+59908_167+59909de...
ENST00000460382.5:c.167+59908_167+59909delinsAT ENSP00000417422.1:n.167+59908_167+59909de...
ENST00000463855.1:c.230+59908_230+59909delinsAT ENSP00000417843.1:n.230+59908_230+59909de...
ENST00000464071.1:c.*523+59908_*523+59909delinsAT ENSP00000418424.1:n.*523+59908_*523+59909...
ENST00000471389.5:c.1364+59908_1364+59909delinsAT ENSP00000418823.1:n.1364+59908_1364+59909...
NM_001080432.2:c.1364+59908_1364+59909delinsAT NP_001073901.1:n.1364+59908_1364+59909del...
XM_011523313.1:c.1394+59908_1394+59909delinsAT XP_011521615.1:n.1394+59908_1394+59909del...
XM_011523316.1:c.1395-14411_1395-14410delinsAT XP_011521618.1:n.1395-14411_1395-14410del...
NM_001363891.1:c.1394+59908_1394+59909delinsAT NP_001350820.1:n.1394+59908_1394+59909del...
NM_001363894.1:c.1427+59908_1427+59909delinsAT NP_001350823.1:n.1427+59908_1427+59909del...
NM_001363896.1:c.1346+37228_1346+37229delinsAT NP_001350825.1:n.1346+37228_1346+37229del...
NM_001363897.1:c.1286+59908_1286+59909delinsAT NP_001350826.1:n.1286+59908_1286+59909del...
NM_001363898.1:c.1250+59908_1250+59909delinsAT NP_001350827.1:n.1250+59908_1250+59909del...
NM_001363899.1:c.1250+59908_1250+59909delinsAT NP_001350828.1:n.1250+59908_1250+59909del...
NM_001363900.1:c.1220+59908_1220+59909delinsAT NP_001350829.1:n.1220+59908_1220+59909del...
NM_001363901.1:c.1220+59908_1220+59909delinsAT NP_001350830.1:n.1220+59908_1220+59909del...
NM_001363903.1:c.1239+105066_1239+105067delinsAT NP_001350832.1:n.1239+105066_1239+105067d...
NM_001363905.1:c.851+59908_851+59909delinsAT NP_001350834.1:n.851+59908_851+59909delin...
NM_001363988.1:c.*22+37228_*22+37229delinsAT NP_001350917.1:n.*22+37228_*22+37229delin...
NR_156761.1:n.614+59908_614+59909delinsAT
XM_011523316.3:c.1395-14411_1395-14410delinsAT XP_011521618.1:n.1395-14411_1395-14410del...
XM_024450437.1:c.1365-14411_1365-14410delinsAT XP_024306205.1:n.1365-14411_1365-14410del...
NM_001080432.3:c.1364+59908_1364+59909delinsAT MANE Select NP_001073901.1:n.1364+59908_1364+59909del...