Canonical Allele Identifier: CA2561370609

Gene: FTO

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53994090T>G , CM000678.2:g.53994090T>G	GRCh38
NC_000016.9:g.54028002T>G , CM000678.1:g.54028002T>G	GRCh37
NC_000016.8:g.52585503T>G	NCBI36
NG_012969.1:g.295128T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000471389.6:c.1364+59981T>G MANE Select	ENSP00000418823.1:n.1364+59981T>G
ENST00000563011.2:c.745-45255T>G
ENST00000612285.2:c.389+59981T>G	ENSP00000490300.1:n.389+59981T>G
ENST00000635892.1:n.214+59981T>G
ENST00000636491.1:c.1347-14338T>G	ENSP00000490047.1:n.1347-14338T>G
ENST00000636992.1:c.1240-19288T>G	ENSP00000489886.1:n.1240-19288T>G
ENST00000637562.1:c.1364+59981T>G	ENSP00000490426.1:n.1364+59981T>G
ENST00000637845.1:c.1364+59981T>G	ENSP00000489638.1:n.1364+59981T>G
ENST00000637969.1:c.1364+59981T>G	ENSP00000490516.1:n.1364+59981T>G
ENST00000268349.7:c.97+9136T>G	ENSP00000268349.7:n.97+9136T>G
ENST00000431610.6:c.167+59981T>G	ENSP00000415636.2:n.167+59981T>G
ENST00000460382.5:c.167+59981T>G	ENSP00000417422.1:n.167+59981T>G
ENST00000463855.1:c.230+59981T>G	ENSP00000417843.1:n.230+59981T>G
ENST00000464071.1:c.*523+59981T>G	ENSP00000418424.1:n.*523+59981T>G
ENST00000471389.5:c.1364+59981T>G	ENSP00000418823.1:n.1364+59981T>G
NM_001080432.2:c.1364+59981T>G	NP_001073901.1:n.1364+59981T>G
XM_011523313.1:c.1394+59981T>G	XP_011521615.1:n.1394+59981T>G
XM_011523316.1:c.1395-14338T>G	XP_011521618.1:n.1395-14338T>G
NM_001363891.1:c.1394+59981T>G	NP_001350820.1:n.1394+59981T>G
NM_001363894.1:c.1427+59981T>G	NP_001350823.1:n.1427+59981T>G
NM_001363896.1:c.1346+37301T>G	NP_001350825.1:n.1346+37301T>G
NM_001363897.1:c.1286+59981T>G	NP_001350826.1:n.1286+59981T>G
NM_001363898.1:c.1250+59981T>G	NP_001350827.1:n.1250+59981T>G
NM_001363899.1:c.1250+59981T>G	NP_001350828.1:n.1250+59981T>G
NM_001363900.1:c.1220+59981T>G	NP_001350829.1:n.1220+59981T>G
NM_001363901.1:c.1220+59981T>G	NP_001350830.1:n.1220+59981T>G
NM_001363903.1:c.1239+105139T>G	NP_001350832.1:n.1239+105139T>G
NM_001363905.1:c.851+59981T>G	NP_001350834.1:n.851+59981T>G
NM_001363988.1:c.*22+37301T>G	NP_001350917.1:n.*22+37301T>G
NR_156761.1:n.614+59981T>G
XM_011523316.3:c.1395-14338T>G	XP_011521618.1:n.1395-14338T>G
XM_024450437.1:c.1365-14338T>G	XP_024306205.1:n.1365-14338T>G
NM_001080432.3:c.1364+59981T>G MANE Select	NP_001073901.1:n.1364+59981T>G