Canonical Allele Identifier: CA2545911677

Gene: FTO

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53993931_53993932insGG , CM000678.2:g.53993931_53993932insGG	GRCh38
NC_000016.9:g.54027843_54027844insGG , CM000678.1:g.54027843_54027844insGG	GRCh37
NC_000016.8:g.52585344_52585345insGG	NCBI36
NG_012969.1:g.294969_294970insGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000471389.6:c.1364+59822_1364+59823insGG MANE Select	ENSP00000418823.1:n.1364+59822_1364+59823insGG
ENST00000563011.2:c.745-45414_745-45413insGG
ENST00000612285.2:c.389+59822_389+59823insGG	ENSP00000490300.1:n.389+59822_389+59823insGG
ENST00000635892.1:n.214+59822_214+59823insGG
ENST00000636491.1:c.1347-14497_1347-14496insGG	ENSP00000490047.1:n.1347-14497_1347-14496insGG
ENST00000636992.1:c.1240-19447_1240-19446insGG	ENSP00000489886.1:n.1240-19447_1240-19446insGG
ENST00000637562.1:c.1364+59822_1364+59823insGG	ENSP00000490426.1:n.1364+59822_1364+59823insGG
ENST00000637845.1:c.1364+59822_1364+59823insGG	ENSP00000489638.1:n.1364+59822_1364+59823insGG
ENST00000637969.1:c.1364+59822_1364+59823insGG	ENSP00000490516.1:n.1364+59822_1364+59823insGG
ENST00000268349.7:c.97+8977_97+8978insGG	ENSP00000268349.7:n.97+8977_97+8978insGG
ENST00000431610.6:c.167+59822_167+59823insGG	ENSP00000415636.2:n.167+59822_167+59823insGG
ENST00000460382.5:c.167+59822_167+59823insGG	ENSP00000417422.1:n.167+59822_167+59823insGG
ENST00000463855.1:c.230+59822_230+59823insGG	ENSP00000417843.1:n.230+59822_230+59823insGG
ENST00000464071.1:c.*523+59822_*523+59823insGG	ENSP00000418424.1:n.*523+59822_*523+59823insGG
ENST00000471389.5:c.1364+59822_1364+59823insGG	ENSP00000418823.1:n.1364+59822_1364+59823insGG
NM_001080432.2:c.1364+59822_1364+59823insGG	NP_001073901.1:n.1364+59822_1364+59823insGG
XM_011523313.1:c.1394+59822_1394+59823insGG	XP_011521615.1:n.1394+59822_1394+59823insGG
XM_011523316.1:c.1395-14497_1395-14496insGG	XP_011521618.1:n.1395-14497_1395-14496insGG
NM_001363891.1:c.1394+59822_1394+59823insGG	NP_001350820.1:n.1394+59822_1394+59823insGG
NM_001363894.1:c.1427+59822_1427+59823insGG	NP_001350823.1:n.1427+59822_1427+59823insGG
NM_001363896.1:c.1346+37142_1346+37143insGG	NP_001350825.1:n.1346+37142_1346+37143insGG
NM_001363897.1:c.1286+59822_1286+59823insGG	NP_001350826.1:n.1286+59822_1286+59823insGG
NM_001363898.1:c.1250+59822_1250+59823insGG	NP_001350827.1:n.1250+59822_1250+59823insGG
NM_001363899.1:c.1250+59822_1250+59823insGG	NP_001350828.1:n.1250+59822_1250+59823insGG
NM_001363900.1:c.1220+59822_1220+59823insGG	NP_001350829.1:n.1220+59822_1220+59823insGG
NM_001363901.1:c.1220+59822_1220+59823insGG	NP_001350830.1:n.1220+59822_1220+59823insGG
NM_001363903.1:c.1239+104980_1239+104981insGG	NP_001350832.1:n.1239+104980_1239+104981insGG
NM_001363905.1:c.851+59822_851+59823insGG	NP_001350834.1:n.851+59822_851+59823insGG
NM_001363988.1:c.*22+37142_*22+37143insGG	NP_001350917.1:n.*22+37142_*22+37143insGG
NR_156761.1:n.614+59822_614+59823insGG
XM_011523316.3:c.1395-14497_1395-14496insGG	XP_011521618.1:n.1395-14497_1395-14496insGG
XM_024450437.1:c.1365-14497_1365-14496insGG	XP_024306205.1:n.1365-14497_1365-14496insGG
NM_001080432.3:c.1364+59822_1364+59823insGG MANE Select	NP_001073901.1:n.1364+59822_1364+59823insGG