Canonical Allele Identifier: CA721682193

Gene: FTO

Linked Data

• dbSNP Id: rs1211187258
• gnomAD v3: 16-53767469-GTTGT-G
• gnomAD v4: 16-53767469-GTTGT-G
• MyVariant Identifiers: chr16:g.53801382_53801385del (hg19) ; chr16:g.53767470_53767473del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53767470_53767473del , CM000678.2:g.53767470_53767473del	GRCh38
NC_000016.9:g.53801382_53801385del , CM000678.1:g.53801382_53801385del	GRCh37
NC_000016.8:g.52358883_52358886del	NCBI36
NG_012969.1:g.68508_68511del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471389.6:c.46-42670_46-42667del MANE Select	ENSP00000418823.1:n.46-42670_46-42667del
ENST00000636030.1:n.73-42670_73-42667del
ENST00000636218.1:c.46-42670_46-42667del	ENSP00000489641.1:n.46-42670_46-42667del
ENST00000636491.1:c.28-42670_28-42667del	ENSP00000490047.1:n.28-42670_28-42667del
ENST00000636992.1:c.46-42670_46-42667del	ENSP00000489886.1:n.46-42670_46-42667del
ENST00000637001.1:c.46-42670_46-42667del	ENSP00000489936.1:n.46-42670_46-42667del
ENST00000637562.1:c.46-42670_46-42667del	ENSP00000490426.1:n.46-42670_46-42667del
ENST00000637845.1:c.46-42670_46-42667del	ENSP00000489638.1:n.46-42670_46-42667del
ENST00000637969.1:c.46-42670_46-42667del	ENSP00000490516.1:n.46-42670_46-42667del
ENST00000640179.1:c.46-42670_46-42667del	ENSP00000490980.1:n.46-42670_46-42667del
ENST00000464071.1:c.46-42670_46-42667del	ENSP00000418424.1:n.46-42670_46-42667del
ENST00000471389.5:c.46-42670_46-42667del	ENSP00000418823.1:n.46-42670_46-42667del
ENST00000570395.1:n.193+3190_193+3193del
NM_001080432.2:c.46-42670_46-42667del	NP_001073901.1:n.46-42670_46-42667del
XM_011523313.1:c.46-42670_46-42667del	XP_011521615.1:n.46-42670_46-42667del
XM_011523314.1:c.46-42670_46-42667del	XP_011521616.1:n.46-42670_46-42667del
XM_011523315.1:c.46-42670_46-42667del	XP_011521617.1:n.46-42670_46-42667del
XM_011523316.1:c.46-42670_46-42667del	XP_011521618.1:n.46-42670_46-42667del
NM_001363891.1:c.46-42670_46-42667del	NP_001350820.1:n.46-42670_46-42667del
NM_001363894.1:c.46-42670_46-42667del	NP_001350823.1:n.46-42670_46-42667del
NM_001363896.1:c.46-42670_46-42667del	NP_001350825.1:n.46-42670_46-42667del
NM_001363897.1:c.46-58394_46-58391del	NP_001350826.1:n.46-58394_46-58391del
NM_001363898.1:c.46-42670_46-42667del	NP_001350827.1:n.46-42670_46-42667del
NM_001363899.1:c.46-42670_46-42667del	NP_001350828.1:n.46-42670_46-42667del
NM_001363900.1:c.46-42670_46-42667del	NP_001350829.1:n.46-42670_46-42667del
NM_001363901.1:c.46-42670_46-42667del	NP_001350830.1:n.46-42670_46-42667del
NM_001363903.1:c.46-42670_46-42667del	NP_001350832.1:n.46-42670_46-42667del
NM_001363905.1:c.-647-42670_-647-42667del	NP_001350834.1:n.-647-42670_-647-42667del
NM_001363988.1:c.46-42670_46-42667del	NP_001350917.1:n.46-42670_46-42667del
NR_156761.1:n.268-42670_268-42667del
XM_011523314.3:c.46-42670_46-42667del	XP_011521616.1:n.46-42670_46-42667del
XM_011523315.3:c.46-42670_46-42667del	XP_011521617.1:n.46-42670_46-42667del
XM_011523316.3:c.46-42670_46-42667del	XP_011521618.1:n.46-42670_46-42667del
XM_017023654.2:c.46-42670_46-42667del	XP_016879143.1:n.46-42670_46-42667del
XM_017023655.2:c.46-42670_46-42667del	XP_016879144.1:n.46-42670_46-42667del
XM_017023656.2:c.46-42670_46-42667del	XP_016879145.1:n.46-42670_46-42667del
XM_017023657.2:c.46-42670_46-42667del	XP_016879146.1:n.46-42670_46-42667del
XM_017023658.2:c.46-42670_46-42667del	XP_016879147.1:n.46-42670_46-42667del
XM_024450437.1:c.46-42670_46-42667del	XP_024306205.1:n.46-42670_46-42667del
XR_002957840.1:n.89-42670_89-42667del
NM_001080432.3:c.46-42670_46-42667del MANE Select	NP_001073901.1:n.46-42670_46-42667del