Canonical Allele Identifier: CA396122020

Gene: FTO

Linked Data

• MyVariant Identifiers: chr16:g.53860154G>A (hg19) ; chr16:g.53826242G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53826242G>A , CM000678.2:g.53826242G>A	GRCh38
NC_000016.9:g.53860154G>A , CM000678.1:g.53860154G>A	GRCh37
NC_000016.8:g.52417655G>A	NCBI36
NG_012969.1:g.127280G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471389.6:c.502G>A MANE Select	ENSP00000418823.1:p.Val168Met
ENST00000636030.1:n.529G>A
ENST00000636218.1:c.502G>A	ENSP00000489641.1:p.Val168Met
ENST00000636491.1:c.484G>A	ENSP00000490047.1:p.Val162Met
ENST00000636992.1:c.502G>A	ENSP00000489886.1:p.Val168Met
ENST00000637001.1:c.502G>A	ENSP00000489936.1:p.Val168Met
ENST00000637562.1:c.502G>A	ENSP00000490426.1:p.Val168Met
ENST00000637845.1:c.502G>A	ENSP00000489638.1:p.Val168Met
ENST00000637969.1:c.502G>A	ENSP00000490516.1:p.Val168Met
ENST00000640179.1:c.123+16025G>A	ENSP00000490980.1:n.123+16025G>A
ENST00000464071.1:c.123+16025G>A	ENSP00000418424.1:n.123+16025G>A
ENST00000471389.5:c.502G>A	ENSP00000418823.1:p.Val168Met
NM_001080432.2:c.502G>A	NP_001073901.1:p.Val168Met
XM_011523313.1:c.502G>A	XP_011521615.1:p.Val168Met
XM_011523314.1:c.502G>A	XP_011521616.1:p.Val168Met
XM_011523315.1:c.502G>A	XP_011521617.1:p.Val168Met
XM_011523316.1:c.502G>A	XP_011521618.1:p.Val168Met
NM_001363891.1:c.502G>A	NP_001350820.1:p.Val168Met
NM_001363894.1:c.502G>A	NP_001350823.1:p.Val168Met
NM_001363896.1:c.502G>A	NP_001350825.1:p.Val168Met
NM_001363897.1:c.424G>A	NP_001350826.1:p.Val142Met
NM_001363898.1:c.502G>A	NP_001350827.1:p.Val168Met
NM_001363899.1:c.502G>A	NP_001350828.1:p.Val168Met
NM_001363900.1:c.502G>A	NP_001350829.1:p.Val168Met
NM_001363901.1:c.502G>A	NP_001350830.1:p.Val168Met
NM_001363903.1:c.502G>A	NP_001350832.1:p.Val168Met
NM_001363905.1:c.-12G>A	NP_001350834.1:n.-12G>A
NM_001363988.1:c.502G>A	NP_001350917.1:p.Val168Met
NR_156761.1:n.345+16025G>A
XM_011523314.3:c.502G>A	XP_011521616.1:p.Val168Met
XM_011523315.3:c.502G>A	XP_011521617.1:p.Val168Met
XM_011523316.3:c.502G>A	XP_011521618.1:p.Val168Met
XM_017023654.2:c.502G>A	XP_016879143.1:p.Val168Met
XM_017023655.2:c.502G>A	XP_016879144.1:p.Val168Met
XM_017023656.2:c.502G>A	XP_016879145.1:p.Val168Met
XM_017023657.2:c.502G>A	XP_016879146.1:p.Val168Met
XM_017023658.2:c.502G>A	XP_016879147.1:p.Val168Met
XM_024450437.1:c.502G>A	XP_024306205.1:p.Val168Met
XR_002957840.1:n.545G>A
NM_001080432.3:c.502G>A MANE Select	NP_001073901.1:p.Val168Met