Canonical Allele Identifier: CA2223283089

Gene: FTO

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53825372_53825375delinsTTAA , CM000678.2:g.53825372_53825375delinsTTAA	GRCh38
NC_000016.9:g.53859284_53859287delinsTTAA , CM000678.1:g.53859284_53859287delinsTTAA	GRCh37
NC_000016.8:g.52416785_52416788delinsTTAA	NCBI36
NG_012969.1:g.126410_126413delinsTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471389.6:c.124-492_124-489delinsTTAA MANE Select	ENSP00000418823.1:n.124-492_124-489delinsTTAA
ENST00000636030.1:n.151-492_151-489delinsTTAA
ENST00000636218.1:c.124-492_124-489delinsTTAA	ENSP00000489641.1:n.124-492_124-489delinsTTAA
ENST00000636491.1:c.106-492_106-489delinsTTAA	ENSP00000490047.1:n.106-492_106-489delinsTTAA
ENST00000636992.1:c.124-492_124-489delinsTTAA	ENSP00000489886.1:n.124-492_124-489delinsTTAA
ENST00000637001.1:c.124-492_124-489delinsTTAA	ENSP00000489936.1:n.124-492_124-489delinsTTAA
ENST00000637562.1:c.124-492_124-489delinsTTAA	ENSP00000490426.1:n.124-492_124-489delinsTTAA
ENST00000637845.1:c.124-492_124-489delinsTTAA	ENSP00000489638.1:n.124-492_124-489delinsTTAA
ENST00000637969.1:c.124-492_124-489delinsTTAA	ENSP00000490516.1:n.124-492_124-489delinsTTAA
ENST00000640179.1:c.123+15155_123+15158delinsTTAA	ENSP00000490980.1:n.123+15155_123+15158delinsTTAA
ENST00000464071.1:c.123+15155_123+15158delinsTTAA	ENSP00000418424.1:n.123+15155_123+15158delinsTTAA
ENST00000471389.5:c.124-492_124-489delinsTTAA	ENSP00000418823.1:n.124-492_124-489delinsTTAA
ENST00000570395.1:n.451-492_451-489delinsTTAA
NM_001080432.2:c.124-492_124-489delinsTTAA	NP_001073901.1:n.124-492_124-489delinsTTAA
XM_011523313.1:c.124-492_124-489delinsTTAA	XP_011521615.1:n.124-492_124-489delinsTTAA
XM_011523314.1:c.124-492_124-489delinsTTAA	XP_011521616.1:n.124-492_124-489delinsTTAA
XM_011523315.1:c.124-492_124-489delinsTTAA	XP_011521617.1:n.124-492_124-489delinsTTAA
XM_011523316.1:c.124-492_124-489delinsTTAA	XP_011521618.1:n.124-492_124-489delinsTTAA
NM_001363891.1:c.124-492_124-489delinsTTAA	NP_001350820.1:n.124-492_124-489delinsTTAA
NM_001363894.1:c.124-492_124-489delinsTTAA	NP_001350823.1:n.124-492_124-489delinsTTAA
NM_001363896.1:c.124-492_124-489delinsTTAA	NP_001350825.1:n.124-492_124-489delinsTTAA
NM_001363897.1:c.46-492_46-489delinsTTAA	NP_001350826.1:n.46-492_46-489delinsTTAA
NM_001363898.1:c.124-492_124-489delinsTTAA	NP_001350827.1:n.124-492_124-489delinsTTAA
NM_001363899.1:c.124-492_124-489delinsTTAA	NP_001350828.1:n.124-492_124-489delinsTTAA
NM_001363900.1:c.124-492_124-489delinsTTAA	NP_001350829.1:n.124-492_124-489delinsTTAA
NM_001363901.1:c.124-492_124-489delinsTTAA	NP_001350830.1:n.124-492_124-489delinsTTAA
NM_001363903.1:c.124-492_124-489delinsTTAA	NP_001350832.1:n.124-492_124-489delinsTTAA
NM_001363905.1:c.-390-492_-390-489delinsTTAA	NP_001350834.1:n.-390-492_-390-489delinsTTAA
NM_001363988.1:c.124-492_124-489delinsTTAA	NP_001350917.1:n.124-492_124-489delinsTTAA
NR_156761.1:n.345+15155_345+15158delinsTTAA
XM_011523314.3:c.124-492_124-489delinsTTAA	XP_011521616.1:n.124-492_124-489delinsTTAA
XM_011523315.3:c.124-492_124-489delinsTTAA	XP_011521617.1:n.124-492_124-489delinsTTAA
XM_011523316.3:c.124-492_124-489delinsTTAA	XP_011521618.1:n.124-492_124-489delinsTTAA
XM_017023654.2:c.124-492_124-489delinsTTAA	XP_016879143.1:n.124-492_124-489delinsTTAA
XM_017023655.2:c.124-492_124-489delinsTTAA	XP_016879144.1:n.124-492_124-489delinsTTAA
XM_017023656.2:c.124-492_124-489delinsTTAA	XP_016879145.1:n.124-492_124-489delinsTTAA
XM_017023657.2:c.124-492_124-489delinsTTAA	XP_016879146.1:n.124-492_124-489delinsTTAA
XM_017023658.2:c.124-492_124-489delinsTTAA	XP_016879147.1:n.124-492_124-489delinsTTAA
XM_024450437.1:c.124-492_124-489delinsTTAA	XP_024306205.1:n.124-492_124-489delinsTTAA
XR_002957840.1:n.167-492_167-489delinsTTAA
NM_001080432.3:c.124-492_124-489delinsTTAA MANE Select	NP_001073901.1:n.124-492_124-489delinsTTAA