Canonical Allele Identifier: CA396122075

Gene: FTO

Linked Data

• MyVariant Identifiers: chr16:g.53860178T>G (hg19) ; chr16:g.53826266T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53826266T>G , CM000678.2:g.53826266T>G	GRCh38
NC_000016.9:g.53860178T>G , CM000678.1:g.53860178T>G	GRCh37
NC_000016.8:g.52417679T>G	NCBI36
NG_012969.1:g.127304T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471389.6:c.526T>G MANE Select	ENSP00000418823.1:p.Phe176Val
ENST00000636030.1:n.553T>G
ENST00000636218.1:c.526T>G	ENSP00000489641.1:p.Phe176Val
ENST00000636491.1:c.508T>G	ENSP00000490047.1:p.Phe170Val
ENST00000636992.1:c.526T>G	ENSP00000489886.1:p.Phe176Val
ENST00000637001.1:c.526T>G	ENSP00000489936.1:p.Phe176Val
ENST00000637562.1:c.526T>G	ENSP00000490426.1:p.Phe176Val
ENST00000637845.1:c.526T>G	ENSP00000489638.1:p.Phe176Val
ENST00000637969.1:c.526T>G	ENSP00000490516.1:p.Phe176Val
ENST00000640179.1:c.123+16049T>G	ENSP00000490980.1:n.123+16049T>G
ENST00000464071.1:c.123+16049T>G	ENSP00000418424.1:n.123+16049T>G
ENST00000471389.5:c.526T>G	ENSP00000418823.1:p.Phe176Val
NM_001080432.2:c.526T>G	NP_001073901.1:p.Phe176Val
XM_011523313.1:c.526T>G	XP_011521615.1:p.Phe176Val
XM_011523314.1:c.526T>G	XP_011521616.1:p.Phe176Val
XM_011523315.1:c.526T>G	XP_011521617.1:p.Phe176Val
XM_011523316.1:c.526T>G	XP_011521618.1:p.Phe176Val
NM_001363891.1:c.526T>G	NP_001350820.1:p.Phe176Val
NM_001363894.1:c.526T>G	NP_001350823.1:p.Phe176Val
NM_001363896.1:c.526T>G	NP_001350825.1:p.Phe176Val
NM_001363897.1:c.448T>G	NP_001350826.1:p.Phe150Val
NM_001363898.1:c.526T>G	NP_001350827.1:p.Phe176Val
NM_001363899.1:c.526T>G	NP_001350828.1:p.Phe176Val
NM_001363900.1:c.526T>G	NP_001350829.1:p.Phe176Val
NM_001363901.1:c.526T>G	NP_001350830.1:p.Phe176Val
NM_001363903.1:c.526T>G	NP_001350832.1:p.Phe176Val
NM_001363905.1:c.13T>G	NP_001350834.1:p.Phe5Val
NM_001363988.1:c.526T>G	NP_001350917.1:p.Phe176Val
NR_156761.1:n.345+16049T>G
XM_011523314.3:c.526T>G	XP_011521616.1:p.Phe176Val
XM_011523315.3:c.526T>G	XP_011521617.1:p.Phe176Val
XM_011523316.3:c.526T>G	XP_011521618.1:p.Phe176Val
XM_017023654.2:c.526T>G	XP_016879143.1:p.Phe176Val
XM_017023655.2:c.526T>G	XP_016879144.1:p.Phe176Val
XM_017023656.2:c.526T>G	XP_016879145.1:p.Phe176Val
XM_017023657.2:c.526T>G	XP_016879146.1:p.Phe176Val
XM_017023658.2:c.526T>G	XP_016879147.1:p.Phe176Val
XM_024450437.1:c.526T>G	XP_024306205.1:p.Phe176Val
XR_002957840.1:n.569T>G
NM_001080432.3:c.526T>G MANE Select	NP_001073901.1:p.Phe176Val