Canonical Allele Identifier: CA721690924

Gene: FTO

Linked Data

• dbSNP Id: rs1234589426
• MyVariant Identifiers: chr16:g.53816052_53816053del (hg19) ; chr16:g.53782140_53782141del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53782140_53782141del , CM000678.2:g.53782140_53782141del	GRCh38
NC_000016.9:g.53816052_53816053del , CM000678.1:g.53816052_53816053del	GRCh37
NC_000016.8:g.52373553_52373554del	NCBI36
NG_012969.1:g.83178_83179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471389.6:c.46-28000_46-27999del MANE Select	ENSP00000418823.1:n.46-28000_46-27999del
ENST00000636030.1:n.73-28000_73-27999del
ENST00000636218.1:c.46-28000_46-27999del	ENSP00000489641.1:n.46-28000_46-27999del
ENST00000636491.1:c.28-28000_28-27999del	ENSP00000490047.1:n.28-28000_28-27999del
ENST00000636992.1:c.46-28000_46-27999del	ENSP00000489886.1:n.46-28000_46-27999del
ENST00000637001.1:c.46-28000_46-27999del	ENSP00000489936.1:n.46-28000_46-27999del
ENST00000637562.1:c.46-28000_46-27999del	ENSP00000490426.1:n.46-28000_46-27999del
ENST00000637845.1:c.46-28000_46-27999del	ENSP00000489638.1:n.46-28000_46-27999del
ENST00000637969.1:c.46-28000_46-27999del	ENSP00000490516.1:n.46-28000_46-27999del
ENST00000640179.1:c.46-28000_46-27999del	ENSP00000490980.1:n.46-28000_46-27999del
ENST00000464071.1:c.46-28000_46-27999del	ENSP00000418424.1:n.46-28000_46-27999del
ENST00000471389.5:c.46-28000_46-27999del	ENSP00000418823.1:n.46-28000_46-27999del
ENST00000570395.1:n.193+17860_193+17861del
NM_001080432.2:c.46-28000_46-27999del	NP_001073901.1:n.46-28000_46-27999del
XM_011523313.1:c.46-28000_46-27999del	XP_011521615.1:n.46-28000_46-27999del
XM_011523314.1:c.46-28000_46-27999del	XP_011521616.1:n.46-28000_46-27999del
XM_011523315.1:c.46-28000_46-27999del	XP_011521617.1:n.46-28000_46-27999del
XM_011523316.1:c.46-28000_46-27999del	XP_011521618.1:n.46-28000_46-27999del
NM_001363891.1:c.46-28000_46-27999del	NP_001350820.1:n.46-28000_46-27999del
NM_001363894.1:c.46-28000_46-27999del	NP_001350823.1:n.46-28000_46-27999del
NM_001363896.1:c.46-28000_46-27999del	NP_001350825.1:n.46-28000_46-27999del
NM_001363897.1:c.46-43724_46-43723del	NP_001350826.1:n.46-43724_46-43723del
NM_001363898.1:c.46-28000_46-27999del	NP_001350827.1:n.46-28000_46-27999del
NM_001363899.1:c.46-28000_46-27999del	NP_001350828.1:n.46-28000_46-27999del
NM_001363900.1:c.46-28000_46-27999del	NP_001350829.1:n.46-28000_46-27999del
NM_001363901.1:c.46-28000_46-27999del	NP_001350830.1:n.46-28000_46-27999del
NM_001363903.1:c.46-28000_46-27999del	NP_001350832.1:n.46-28000_46-27999del
NM_001363905.1:c.-647-28000_-647-27999del	NP_001350834.1:n.-647-28000_-647-27999del
NM_001363988.1:c.46-28000_46-27999del	NP_001350917.1:n.46-28000_46-27999del
NR_156761.1:n.268-28000_268-27999del
XM_011523314.3:c.46-28000_46-27999del	XP_011521616.1:n.46-28000_46-27999del
XM_011523315.3:c.46-28000_46-27999del	XP_011521617.1:n.46-28000_46-27999del
XM_011523316.3:c.46-28000_46-27999del	XP_011521618.1:n.46-28000_46-27999del
XM_017023654.2:c.46-28000_46-27999del	XP_016879143.1:n.46-28000_46-27999del
XM_017023655.2:c.46-28000_46-27999del	XP_016879144.1:n.46-28000_46-27999del
XM_017023656.2:c.46-28000_46-27999del	XP_016879145.1:n.46-28000_46-27999del
XM_017023657.2:c.46-28000_46-27999del	XP_016879146.1:n.46-28000_46-27999del
XM_017023658.2:c.46-28000_46-27999del	XP_016879147.1:n.46-28000_46-27999del
XM_024450437.1:c.46-28000_46-27999del	XP_024306205.1:n.46-28000_46-27999del
XR_002957840.1:n.89-28000_89-27999del
NM_001080432.3:c.46-28000_46-27999del MANE Select	NP_001073901.1:n.46-28000_46-27999del