Canonical Allele Identifier: CA8058624

Gene: FTO

Linked Data

• ClinVar Variation Id: 235247
• ClinVar RCV Id: RCV000224338
• dbSNP Id: rs376381270
• ExAC: 16:54145674 G / T
• gnomAD v2: 16-54145674-G-T
• gnomAD v3: 16-54111762-G-T
• gnomAD v4: 16-54111762-G-T
• MyVariant Identifiers: chr16:g.54145674G>T (hg19) ; chr16:g.54111762G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.54111762G>T , CM000678.2:g.54111762G>T	GRCh38
NC_000016.9:g.54145674G>T , CM000678.1:g.54145674G>T	GRCh37
NC_000016.8:g.52703175G>T	NCBI36
NG_012969.1:g.412800G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471389.6:c.1365G>T MANE Select	ENSP00000418823.1:p.Arg455Ser
ENST00000612285.2:c.390G>T	ENSP00000490300.1:p.Arg130Ser
ENST00000635892.1:n.215G>T
ENST00000636091.1:n.2646G>T
ENST00000636992.1:c.*108G>T	ENSP00000489886.1:n.*108G>T
ENST00000637562.1:c.*56G>T	ENSP00000490426.1:n.*56G>T
ENST00000637845.1:c.1365G>T	ENSP00000489638.1:p.Arg455Ser
ENST00000637969.1:c.1365G>T	ENSP00000490516.1:p.Arg455Ser
ENST00000268349.7:c.98G>T	ENSP00000268349.7:p.Gly33Val
ENST00000431610.6:c.168G>T	ENSP00000415636.2:p.Arg56Ser
ENST00000460382.5:c.168G>T	ENSP00000417422.1:p.Arg56Ser
ENST00000463855.1:c.231G>T	ENSP00000417843.1:p.Arg77Ser
ENST00000464071.1:c.*524G>T	ENSP00000418424.1:n.*524G>T
ENST00000471389.5:c.1365G>T	ENSP00000418823.1:p.Arg455Ser
ENST00000472835.1:n.307G>T
NM_001080432.2:c.1365G>T	NP_001073901.1:p.Arg455Ser
XM_011523313.1:c.1395G>T	XP_011521615.1:p.Arg465Ser
NM_001363891.1:c.1395G>T	NP_001350820.1:p.Arg465Ser
NM_001363894.1:c.1428G>T	NP_001350823.1:p.Arg476Ser
NM_001363896.1:c.1347G>T	NP_001350825.1:p.Arg449Ser
NM_001363897.1:c.1287G>T	NP_001350826.1:p.Arg429Ser
NM_001363898.1:c.1251G>T	NP_001350827.1:p.Arg417Ser
NM_001363899.1:c.1251G>T	NP_001350828.1:p.Arg417Ser
NM_001363900.1:c.1221G>T	NP_001350829.1:p.Arg407Ser
NM_001363901.1:c.1221G>T	NP_001350830.1:p.Arg407Ser
NM_001363903.1:c.1240G>T	NP_001350832.1:p.Val414Leu
NM_001363905.1:c.852G>T	NP_001350834.1:p.Arg284Ser
NM_001363988.1:c.*23G>T	NP_001350917.1:n.*23G>T
NR_156761.1:n.615G>T
NM_001080432.3:c.1365G>T MANE Select	NP_001073901.1:p.Arg455Ser