Canonical Allele Identifier: CA10647730

Gene: FTO

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.54113826del , CM000678.2:g.54113826del	GRCh38
NC_000016.9:g.54147738del , CM000678.1:g.54147738del	GRCh37
NC_000016.8:g.52705239del	NCBI36
NG_012969.1:g.414864del

Transcript Alleles

HGVS	Amino-acid Change
NM_001080432.3:c.*1911del MANE Select	NP_001073901.1:n.*1911del
ENST00000471389.6:c.*1911del MANE Select	ENSP00000418823.1:n.*1911del
NM_001080432.2:c.*1911del	NP_001073901.1:n.*1911del
NM_001363891.1:c.*1911del	NP_001350820.1:n.*1911del
NM_001363894.1:c.*1911del	NP_001350823.1:n.*1911del
NM_001363896.1:c.*1911del	NP_001350825.1:n.*1911del
NM_001363897.1:c.*1911del	NP_001350826.1:n.*1911del
NM_001363898.1:c.*1911del	NP_001350827.1:n.*1911del
NM_001363899.1:c.*1911del	NP_001350828.1:n.*1911del
NM_001363900.1:c.*1911del	NP_001350829.1:n.*1911del
NM_001363901.1:c.*1911del	NP_001350830.1:n.*1911del
NM_001363903.1:c.*2029del	NP_001350832.1:n.*2029del
NM_001363905.1:c.*1911del	NP_001350834.1:n.*1911del
NM_001363988.1:c.*2087del	NP_001350917.1:n.*2087del
NR_156761.1:n.2679del
ENST00000268349.7:c.2162del	ENSP00000268349.7:n.2162del
ENST00000463855.1:c.*1911del	ENSP00000417843.1:n.*1911del
ENST00000471389.5:c.*1911del	ENSP00000418823.1:n.*1911del
ENST00000612285.2:c.517+1937del	ENSP00000490300.1:n.517+1937del
ENST00000636091.1:n.4710del
ENST00000637845.1:c.1492+1937del	ENSP00000489638.1:n.1492+1937del
ENST00000637969.1:c.1492+1937del	ENSP00000490516.1:n.1492+1937del
XM_011523313.1:c.*1911del	XP_011521615.1:n.*1911del