Canonical Allele Identifier: CA2507562109

Gene: FTO

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.54104986_54104987insTAAA , CM000678.2:g.54104986_54104987insTAAA	GRCh38
NC_000016.9:g.54138898_54138899insTAAA , CM000678.1:g.54138898_54138899insTAAA	GRCh37
NC_000016.8:g.52696399_52696400insTAAA	NCBI36
NG_012969.1:g.406024_406025insTAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000471389.6:c.1365-6776_1365-6775insTAAA MANE Select	ENSP00000418823.1:n.1365-6776_1365-6775in...
ENST00000612285.2:c.390-6776_390-6775insTAAA	ENSP00000490300.1:n.390-6776_390-6775insT...
ENST00000635892.1:n.215-6776_215-6775insTAAA
ENST00000636091.1:n.2646-6776_2646-6775insTAAA
ENST00000636992.1:c.*108-6776_*108-6775insTAAA	ENSP00000489886.1:n.*108-6776_*108-6775in...
ENST00000637562.1:c.*56-6776_*56-6775insTAAA	ENSP00000490426.1:n.*56-6776_*56-6775insT...
ENST00000637845.1:c.1365-6776_1365-6775insTAAA	ENSP00000489638.1:n.1365-6776_1365-6775in...
ENST00000637969.1:c.1365-6776_1365-6775insTAAA	ENSP00000490516.1:n.1365-6776_1365-6775in...
ENST00000268349.7:c.98-6776_98-6775insTAAA	ENSP00000268349.7:n.98-6776_98-6775insTAA...
ENST00000431610.6:c.168-6776_168-6775insTAAA	ENSP00000415636.2:n.168-6776_168-6775insT...
ENST00000460382.5:c.168-6776_168-6775insTAAA	ENSP00000417422.1:n.168-6776_168-6775insT...
ENST00000463855.1:c.231-6776_231-6775insTAAA	ENSP00000417843.1:n.231-6776_231-6775insT...
ENST00000464071.1:c.*524-6776_*524-6775insTAAA	ENSP00000418424.1:n.*524-6776_*524-6775in...
ENST00000471389.5:c.1365-6776_1365-6775insTAAA	ENSP00000418823.1:n.1365-6776_1365-6775in...
ENST00000472835.1:n.307-6776_307-6775insTAAA
NM_001080432.2:c.1365-6776_1365-6775insTAAA	NP_001073901.1:n.1365-6776_1365-6775insTA...
XM_011523313.1:c.1395-6776_1395-6775insTAAA	XP_011521615.1:n.1395-6776_1395-6775insTA...
NM_001363891.1:c.1395-6776_1395-6775insTAAA	NP_001350820.1:n.1395-6776_1395-6775insTA...
NM_001363894.1:c.1428-6776_1428-6775insTAAA	NP_001350823.1:n.1428-6776_1428-6775insTA...
NM_001363896.1:c.1347-6776_1347-6775insTAAA	NP_001350825.1:n.1347-6776_1347-6775insTA...
NM_001363897.1:c.1287-6776_1287-6775insTAAA	NP_001350826.1:n.1287-6776_1287-6775insTA...
NM_001363898.1:c.1251-6776_1251-6775insTAAA	NP_001350827.1:n.1251-6776_1251-6775insTA...
NM_001363899.1:c.1251-6776_1251-6775insTAAA	NP_001350828.1:n.1251-6776_1251-6775insTA...
NM_001363900.1:c.1221-6776_1221-6775insTAAA	NP_001350829.1:n.1221-6776_1221-6775insTA...
NM_001363901.1:c.1221-6776_1221-6775insTAAA	NP_001350830.1:n.1221-6776_1221-6775insTA...
NM_001363903.1:c.1240-6776_1240-6775insTAAA	NP_001350832.1:n.1240-6776_1240-6775insTA...
NM_001363905.1:c.852-6776_852-6775insTAAA	NP_001350834.1:n.852-6776_852-6775insTAAA...
NM_001363988.1:c.*23-6776_*23-6775insTAAA	NP_001350917.1:n.*23-6776_*23-6775insTAAA...
NR_156761.1:n.615-6776_615-6775insTAAA
NM_001080432.3:c.1365-6776_1365-6775insTAAA MANE Select	NP_001073901.1:n.1365-6776_1365-6775insTA...