Canonical Allele Identifier: CA8058550

Gene: FTO

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53888885G>A , CM000678.2:g.53888885G>A	GRCh38
NC_000016.9:g.53922797G>A , CM000678.1:g.53922797G>A	GRCh37
NC_000016.8:g.52480298G>A	NCBI36
NG_012969.1:g.189923G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471389.6:c.1173G>A MANE Select	ENSP00000418823.1:p.Lys391=
ENST00000563011.2:c.553G>A
ENST00000612285.2:c.198G>A	ENSP00000490300.1:p.Lys66=
ENST00000636030.1:n.1200G>A
ENST00000636218.1:c.1173G>A	ENSP00000489641.1:p.Lys391=
ENST00000636491.1:c.1155G>A	ENSP00000490047.1:p.Lys385=
ENST00000636992.1:c.1173G>A	ENSP00000489886.1:p.Lys391=
ENST00000637001.1:c.1173G>A	ENSP00000489936.1:p.Lys391=
ENST00000637562.1:c.1173G>A	ENSP00000490426.1:p.Lys391=
ENST00000637845.1:c.1173G>A	ENSP00000489638.1:p.Lys391=
ENST00000637969.1:c.1173G>A	ENSP00000490516.1:p.Lys391=
ENST00000431610.6:c.-25G>A	ENSP00000415636.2:n.-25G>A
ENST00000460382.5:c.-25G>A	ENSP00000417422.1:n.-25G>A
ENST00000464071.1:c.*332G>A	ENSP00000418424.1:n.*332G>A
ENST00000471389.5:c.1173G>A	ENSP00000418823.1:p.Lys391=
NM_001080432.2:c.1173G>A	NP_001073901.1:p.Lys391=
XM_011523313.1:c.1203G>A	XP_011521615.1:p.Lys401=
XM_011523314.1:c.1203G>A	XP_011521616.1:p.Lys401=
XM_011523315.1:c.1203G>A	XP_011521617.1:p.Lys401=
XM_011523316.1:c.1203G>A	XP_011521618.1:p.Lys401=
NM_001363891.1:c.1203G>A	NP_001350820.1:p.Lys401=
NM_001363894.1:c.1173G>A	NP_001350823.1:p.Lys391=
NM_001363896.1:c.1173G>A	NP_001350825.1:p.Lys391=
NM_001363897.1:c.1095G>A	NP_001350826.1:p.Lys365=
NM_001363898.1:c.1059G>A	NP_001350827.1:p.Lys353=
NM_001363899.1:c.1059G>A	NP_001350828.1:p.Lys353=
NM_001363900.1:c.1029G>A	NP_001350829.1:p.Lys343=
NM_001363901.1:c.1029G>A	NP_001350830.1:p.Lys343=
NM_001363903.1:c.1173G>A	NP_001350832.1:p.Lys391=
NM_001363905.1:c.660G>A	NP_001350834.1:p.Lys220=
NM_001363988.1:c.1173G>A	NP_001350917.1:p.Lys391=
NR_156761.1:n.489+44587G>A
XM_011523314.3:c.1203G>A	XP_011521616.1:p.Lys401=
XM_011523315.3:c.1203G>A	XP_011521617.1:p.Lys401=
XM_011523316.3:c.1203G>A	XP_011521618.1:p.Lys401=
XM_017023654.2:c.1203G>A	XP_016879143.1:p.Lys401=
XM_017023655.2:c.1173G>A	XP_016879144.1:p.Lys391=
XM_017023656.2:c.1173G>A	XP_016879145.1:p.Lys391=
XM_017023657.2:c.1173G>A	XP_016879146.1:p.Lys391=
XM_024450437.1:c.1173G>A	XP_024306205.1:p.Lys391=
NM_001080432.3:c.1173G>A MANE Select	NP_001073901.1:p.Lys391=