Canonical Allele Identifier: CA2497399062

Gene: FTO

Linked Data

• dbSNP Id: rs2086714981

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.54104899_54104903del , CM000678.2:g.54104899_54104903del	GRCh38
NC_000016.9:g.54138811_54138815del , CM000678.1:g.54138811_54138815del	GRCh37
NC_000016.8:g.52696312_52696316del	NCBI36
NG_012969.1:g.405937_405941del

Transcript Alleles

HGVS	Amino-acid change
ENST00000471389.6:c.1365-6863_1365-6859del MANE Select	ENSP00000418823.1:n.1365-6863_1365-6859de...
ENST00000612285.2:c.390-6863_390-6859del	ENSP00000490300.1:n.390-6863_390-6859del
ENST00000635892.1:n.215-6863_215-6859del
ENST00000636091.1:n.2646-6863_2646-6859del
ENST00000636992.1:c.*108-6863_*108-6859del	ENSP00000489886.1:n.*108-6863_*108-6859de...
ENST00000637562.1:c.*56-6863_*56-6859del	ENSP00000490426.1:n.*56-6863_*56-6859del
ENST00000637845.1:c.1365-6863_1365-6859del	ENSP00000489638.1:n.1365-6863_1365-6859de...
ENST00000637969.1:c.1365-6863_1365-6859del	ENSP00000490516.1:n.1365-6863_1365-6859de...
ENST00000268349.7:c.98-6863_98-6859del	ENSP00000268349.7:n.98-6863_98-6859del
ENST00000431610.6:c.168-6863_168-6859del	ENSP00000415636.2:n.168-6863_168-6859del
ENST00000460382.5:c.168-6863_168-6859del	ENSP00000417422.1:n.168-6863_168-6859del
ENST00000463855.1:c.231-6863_231-6859del	ENSP00000417843.1:n.231-6863_231-6859del
ENST00000464071.1:c.*524-6863_*524-6859del	ENSP00000418424.1:n.*524-6863_*524-6859de...
ENST00000471389.5:c.1365-6863_1365-6859del	ENSP00000418823.1:n.1365-6863_1365-6859de...
ENST00000472835.1:n.307-6863_307-6859del
NM_001080432.2:c.1365-6863_1365-6859del	NP_001073901.1:n.1365-6863_1365-6859del
XM_011523313.1:c.1395-6863_1395-6859del	XP_011521615.1:n.1395-6863_1395-6859del
NM_001363891.1:c.1395-6863_1395-6859del	NP_001350820.1:n.1395-6863_1395-6859del
NM_001363894.1:c.1428-6863_1428-6859del	NP_001350823.1:n.1428-6863_1428-6859del
NM_001363896.1:c.1347-6863_1347-6859del	NP_001350825.1:n.1347-6863_1347-6859del
NM_001363897.1:c.1287-6863_1287-6859del	NP_001350826.1:n.1287-6863_1287-6859del
NM_001363898.1:c.1251-6863_1251-6859del	NP_001350827.1:n.1251-6863_1251-6859del
NM_001363899.1:c.1251-6863_1251-6859del	NP_001350828.1:n.1251-6863_1251-6859del
NM_001363900.1:c.1221-6863_1221-6859del	NP_001350829.1:n.1221-6863_1221-6859del
NM_001363901.1:c.1221-6863_1221-6859del	NP_001350830.1:n.1221-6863_1221-6859del
NM_001363903.1:c.1240-6863_1240-6859del	NP_001350832.1:n.1240-6863_1240-6859del
NM_001363905.1:c.852-6863_852-6859del	NP_001350834.1:n.852-6863_852-6859del
NM_001363988.1:c.*23-6863_*23-6859del	NP_001350917.1:n.*23-6863_*23-6859del
NR_156761.1:n.615-6863_615-6859del
NM_001080432.3:c.1365-6863_1365-6859del MANE Select	NP_001073901.1:n.1365-6863_1365-6859del