Canonical Allele Identifier: CA977446619

Gene: FTO

Linked Data

• dbSNP Id: rs2151524014
• gnomAD v3: 16-53735876-T-TG
• gnomAD v4: 16-53735876-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53735876_53735877insG , CM000678.2:g.53735876_53735877insG	GRCh38
NC_000016.9:g.53769788_53769789insG , CM000678.1:g.53769788_53769789insG	GRCh37
NC_000016.8:g.52327289_52327290insG	NCBI36
NG_012969.1:g.36914_36915insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471389.6:c.45+31647_45+31648insG MANE Select	ENSP00000418823.1:n.45+31647_45+31648insG
ENST00000636030.1:n.72+31647_72+31648insG
ENST00000636218.1:c.45+31647_45+31648insG	ENSP00000489641.1:n.45+31647_45+31648insG
ENST00000636491.1:c.27+24422_27+24423insG	ENSP00000490047.1:n.27+24422_27+24423insG
ENST00000636992.1:c.45+31647_45+31648insG	ENSP00000489886.1:n.45+31647_45+31648insG
ENST00000637001.1:c.45+31647_45+31648insG	ENSP00000489936.1:n.45+31647_45+31648insG
ENST00000637562.1:c.45+31647_45+31648insG	ENSP00000490426.1:n.45+31647_45+31648insG
ENST00000637845.1:c.45+31647_45+31648insG	ENSP00000489638.1:n.45+31647_45+31648insG
ENST00000637969.1:c.45+31647_45+31648insG	ENSP00000490516.1:n.45+31647_45+31648insG
ENST00000640179.1:c.45+31647_45+31648insG	ENSP00000490980.1:n.45+31647_45+31648insG
ENST00000464071.1:c.45+31647_45+31648insG	ENSP00000418424.1:n.45+31647_45+31648insG
ENST00000471389.5:c.45+31647_45+31648insG	ENSP00000418823.1:n.45+31647_45+31648insG
ENST00000570395.1:n.75-28286_75-28285insG
NM_001080432.2:c.45+31647_45+31648insG	NP_001073901.1:n.45+31647_45+31648insG
XM_011523313.1:c.45+31647_45+31648insG	XP_011521615.1:n.45+31647_45+31648insG
XM_011523314.1:c.45+31647_45+31648insG	XP_011521616.1:n.45+31647_45+31648insG
XM_011523315.1:c.45+31647_45+31648insG	XP_011521617.1:n.45+31647_45+31648insG
XM_011523316.1:c.45+31647_45+31648insG	XP_011521618.1:n.45+31647_45+31648insG
NM_001363891.1:c.45+31647_45+31648insG	NP_001350820.1:n.45+31647_45+31648insG
NM_001363894.1:c.45+31647_45+31648insG	NP_001350823.1:n.45+31647_45+31648insG
NM_001363896.1:c.45+31647_45+31648insG	NP_001350825.1:n.45+31647_45+31648insG
NM_001363897.1:c.45+31647_45+31648insG	NP_001350826.1:n.45+31647_45+31648insG
NM_001363898.1:c.45+31647_45+31648insG	NP_001350827.1:n.45+31647_45+31648insG
NM_001363899.1:c.45+31647_45+31648insG	NP_001350828.1:n.45+31647_45+31648insG
NM_001363900.1:c.45+31647_45+31648insG	NP_001350829.1:n.45+31647_45+31648insG
NM_001363901.1:c.45+31647_45+31648insG	NP_001350830.1:n.45+31647_45+31648insG
NM_001363903.1:c.45+31647_45+31648insG	NP_001350832.1:n.45+31647_45+31648insG
NM_001363905.1:c.-648+31647_-648+31648insG	NP_001350834.1:n.-648+31647_-648+31648insG
NM_001363988.1:c.45+31647_45+31648insG	NP_001350917.1:n.45+31647_45+31648insG
NR_156761.1:n.267+31647_267+31648insG
XM_011523314.3:c.45+31647_45+31648insG	XP_011521616.1:n.45+31647_45+31648insG
XM_011523315.3:c.45+31647_45+31648insG	XP_011521617.1:n.45+31647_45+31648insG
XM_011523316.3:c.45+31647_45+31648insG	XP_011521618.1:n.45+31647_45+31648insG
XM_017023654.2:c.45+31647_45+31648insG	XP_016879143.1:n.45+31647_45+31648insG
XM_017023655.2:c.45+31647_45+31648insG	XP_016879144.1:n.45+31647_45+31648insG
XM_017023656.2:c.45+31647_45+31648insG	XP_016879145.1:n.45+31647_45+31648insG
XM_017023657.2:c.45+31647_45+31648insG	XP_016879146.1:n.45+31647_45+31648insG
XM_017023658.2:c.45+31647_45+31648insG	XP_016879147.1:n.45+31647_45+31648insG
XM_024450437.1:c.45+31647_45+31648insG	XP_024306205.1:n.45+31647_45+31648insG
XR_002957840.1:n.88+31647_88+31648insG
NM_001080432.3:c.45+31647_45+31648insG MANE Select	NP_001073901.1:n.45+31647_45+31648insG