Canonical Allele Identifier: CA2223441259
Gene: FTO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.53994091A= , CM000678.2:g.53994091A= GRCh38
NC_000016.9:g.54028003A= , CM000678.1:g.54028003A= GRCh37
NC_000016.8:g.52585504A= NCBI36
NG_012969.1:g.295129A=

Transcript Alleles

HGVS Amino-acid change
ENST00000471389.6:c.1364+59982A= MANE Select ENSP00000418823.1:n.1364+59982A=
ENST00000563011.2:c.745-45254A=
ENST00000612285.2:c.389+59982A= ENSP00000490300.1:n.389+59982A=
ENST00000635892.1:n.214+59982A=
ENST00000636491.1:c.1347-14337A= ENSP00000490047.1:n.1347-14337A=
ENST00000636992.1:c.1240-19287A= ENSP00000489886.1:n.1240-19287A=
ENST00000637562.1:c.1364+59982A= ENSP00000490426.1:n.1364+59982A=
ENST00000637845.1:c.1364+59982A= ENSP00000489638.1:n.1364+59982A=
ENST00000637969.1:c.1364+59982A= ENSP00000490516.1:n.1364+59982A=
ENST00000268349.7:c.97+9137A= ENSP00000268349.7:n.97+9137A=
ENST00000431610.6:c.167+59982A= ENSP00000415636.2:n.167+59982A=
ENST00000460382.5:c.167+59982A= ENSP00000417422.1:n.167+59982A=
ENST00000463855.1:c.230+59982A= ENSP00000417843.1:n.230+59982A=
ENST00000464071.1:c.*523+59982A= ENSP00000418424.1:n.*523+59982A=
ENST00000471389.5:c.1364+59982A= ENSP00000418823.1:n.1364+59982A=
NM_001080432.2:c.1364+59982A= NP_001073901.1:n.1364+59982A=
XM_011523313.1:c.1394+59982A= XP_011521615.1:n.1394+59982A=
XM_011523316.1:c.1395-14337A= XP_011521618.1:n.1395-14337A=
NM_001363891.1:c.1394+59982A= NP_001350820.1:n.1394+59982A=
NM_001363894.1:c.1427+59982A= NP_001350823.1:n.1427+59982A=
NM_001363896.1:c.1346+37302A= NP_001350825.1:n.1346+37302A=
NM_001363897.1:c.1286+59982A= NP_001350826.1:n.1286+59982A=
NM_001363898.1:c.1250+59982A= NP_001350827.1:n.1250+59982A=
NM_001363899.1:c.1250+59982A= NP_001350828.1:n.1250+59982A=
NM_001363900.1:c.1220+59982A= NP_001350829.1:n.1220+59982A=
NM_001363901.1:c.1220+59982A= NP_001350830.1:n.1220+59982A=
NM_001363903.1:c.1239+105140A= NP_001350832.1:n.1239+105140A=
NM_001363905.1:c.851+59982A= NP_001350834.1:n.851+59982A=
NM_001363988.1:c.*22+37302A= NP_001350917.1:n.*22+37302A=
NR_156761.1:n.614+59982A=
XM_011523316.3:c.1395-14337A= XP_011521618.1:n.1395-14337A=
XM_024450437.1:c.1365-14337A= XP_024306205.1:n.1365-14337A=
NM_001080432.3:c.1364+59982A= MANE Select NP_001073901.1:n.1364+59982A=