Canonical Allele Identifier: CA2544250926

Gene: FTO

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53993928_53993929del , CM000678.2:g.53993928_53993929del	GRCh38
NC_000016.9:g.54027840_54027841del , CM000678.1:g.54027840_54027841del	GRCh37
NC_000016.8:g.52585341_52585342del	NCBI36
NG_012969.1:g.294966_294967del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471389.6:c.1364+59819_1364+59820del MANE Select	ENSP00000418823.1:n.1364+59819_1364+59820del
ENST00000563011.2:c.745-45417_745-45416del
ENST00000612285.2:c.389+59819_389+59820del	ENSP00000490300.1:n.389+59819_389+59820del
ENST00000635892.1:n.214+59819_214+59820del
ENST00000636491.1:c.1347-14500_1347-14499del	ENSP00000490047.1:n.1347-14500_1347-14499del
ENST00000636992.1:c.1240-19450_1240-19449del	ENSP00000489886.1:n.1240-19450_1240-19449del
ENST00000637562.1:c.1364+59819_1364+59820del	ENSP00000490426.1:n.1364+59819_1364+59820del
ENST00000637845.1:c.1364+59819_1364+59820del	ENSP00000489638.1:n.1364+59819_1364+59820del
ENST00000637969.1:c.1364+59819_1364+59820del	ENSP00000490516.1:n.1364+59819_1364+59820del
ENST00000268349.7:c.97+8974_97+8975del	ENSP00000268349.7:n.97+8974_97+8975del
ENST00000431610.6:c.167+59819_167+59820del	ENSP00000415636.2:n.167+59819_167+59820del
ENST00000460382.5:c.167+59819_167+59820del	ENSP00000417422.1:n.167+59819_167+59820del
ENST00000463855.1:c.230+59819_230+59820del	ENSP00000417843.1:n.230+59819_230+59820del
ENST00000464071.1:c.*523+59819_*523+59820del	ENSP00000418424.1:n.*523+59819_*523+59820del
ENST00000471389.5:c.1364+59819_1364+59820del	ENSP00000418823.1:n.1364+59819_1364+59820del
NM_001080432.2:c.1364+59819_1364+59820del	NP_001073901.1:n.1364+59819_1364+59820del
XM_011523313.1:c.1394+59819_1394+59820del	XP_011521615.1:n.1394+59819_1394+59820del
XM_011523316.1:c.1395-14500_1395-14499del	XP_011521618.1:n.1395-14500_1395-14499del
NM_001363891.1:c.1394+59819_1394+59820del	NP_001350820.1:n.1394+59819_1394+59820del
NM_001363894.1:c.1427+59819_1427+59820del	NP_001350823.1:n.1427+59819_1427+59820del
NM_001363896.1:c.1346+37139_1346+37140del	NP_001350825.1:n.1346+37139_1346+37140del
NM_001363897.1:c.1286+59819_1286+59820del	NP_001350826.1:n.1286+59819_1286+59820del
NM_001363898.1:c.1250+59819_1250+59820del	NP_001350827.1:n.1250+59819_1250+59820del
NM_001363899.1:c.1250+59819_1250+59820del	NP_001350828.1:n.1250+59819_1250+59820del
NM_001363900.1:c.1220+59819_1220+59820del	NP_001350829.1:n.1220+59819_1220+59820del
NM_001363901.1:c.1220+59819_1220+59820del	NP_001350830.1:n.1220+59819_1220+59820del
NM_001363903.1:c.1239+104977_1239+104978del	NP_001350832.1:n.1239+104977_1239+104978del
NM_001363905.1:c.851+59819_851+59820del	NP_001350834.1:n.851+59819_851+59820del
NM_001363988.1:c.*22+37139_*22+37140del	NP_001350917.1:n.*22+37139_*22+37140del
NR_156761.1:n.614+59819_614+59820del
XM_011523316.3:c.1395-14500_1395-14499del	XP_011521618.1:n.1395-14500_1395-14499del
XM_024450437.1:c.1365-14500_1365-14499del	XP_024306205.1:n.1365-14500_1365-14499del
NM_001080432.3:c.1364+59819_1364+59820del MANE Select	NP_001073901.1:n.1364+59819_1364+59820del