Canonical Allele Identifier: CA622572260

Gene: FTO

Linked Data

• dbSNP Id: rs1287082342
• gnomAD v2: 16-53859121-GTGAGTTCTC-G
• gnomAD v3: 16-53825209-GTGAGTTCTC-G
• gnomAD v4: 16-53825209-GTGAGTTCTC-G
• MyVariant Identifiers: chr16:g.53859122_53859130del (hg19) ; chr16:g.53825210_53825218del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53825211_53825219del , CM000678.2:g.53825211_53825219del	GRCh38
NC_000016.9:g.53859123_53859131del , CM000678.1:g.53859123_53859131del	GRCh37
NC_000016.8:g.52416624_52416632del	NCBI36
NG_012969.1:g.126249_126257del

Transcript Alleles

HGVS	Amino-acid change
ENST00000471389.6:c.124-653_124-645del MANE Select	ENSP00000418823.1:n.124-653_124-645del
ENST00000636030.1:n.151-653_151-645del
ENST00000636218.1:c.124-653_124-645del	ENSP00000489641.1:n.124-653_124-645del
ENST00000636491.1:c.106-653_106-645del	ENSP00000490047.1:n.106-653_106-645del
ENST00000636992.1:c.124-653_124-645del	ENSP00000489886.1:n.124-653_124-645del
ENST00000637001.1:c.124-653_124-645del	ENSP00000489936.1:n.124-653_124-645del
ENST00000637562.1:c.124-653_124-645del	ENSP00000490426.1:n.124-653_124-645del
ENST00000637845.1:c.124-653_124-645del	ENSP00000489638.1:n.124-653_124-645del
ENST00000637969.1:c.124-653_124-645del	ENSP00000490516.1:n.124-653_124-645del
ENST00000640179.1:c.123+14994_123+15002del	ENSP00000490980.1:n.123+14994_123+15002del
ENST00000464071.1:c.123+14994_123+15002del	ENSP00000418424.1:n.123+14994_123+15002del
ENST00000471389.5:c.124-653_124-645del	ENSP00000418823.1:n.124-653_124-645del
ENST00000570395.1:n.451-653_451-645del
NM_001080432.2:c.124-653_124-645del	NP_001073901.1:n.124-653_124-645del
XM_011523313.1:c.124-653_124-645del	XP_011521615.1:n.124-653_124-645del
XM_011523314.1:c.124-653_124-645del	XP_011521616.1:n.124-653_124-645del
XM_011523315.1:c.124-653_124-645del	XP_011521617.1:n.124-653_124-645del
XM_011523316.1:c.124-653_124-645del	XP_011521618.1:n.124-653_124-645del
NM_001363891.1:c.124-653_124-645del	NP_001350820.1:n.124-653_124-645del
NM_001363894.1:c.124-653_124-645del	NP_001350823.1:n.124-653_124-645del
NM_001363896.1:c.124-653_124-645del	NP_001350825.1:n.124-653_124-645del
NM_001363897.1:c.46-653_46-645del	NP_001350826.1:n.46-653_46-645del
NM_001363898.1:c.124-653_124-645del	NP_001350827.1:n.124-653_124-645del
NM_001363899.1:c.124-653_124-645del	NP_001350828.1:n.124-653_124-645del
NM_001363900.1:c.124-653_124-645del	NP_001350829.1:n.124-653_124-645del
NM_001363901.1:c.124-653_124-645del	NP_001350830.1:n.124-653_124-645del
NM_001363903.1:c.124-653_124-645del	NP_001350832.1:n.124-653_124-645del
NM_001363905.1:c.-390-653_-390-645del	NP_001350834.1:n.-390-653_-390-645del
NM_001363988.1:c.124-653_124-645del	NP_001350917.1:n.124-653_124-645del
NR_156761.1:n.345+14994_345+15002del
XM_011523314.3:c.124-653_124-645del	XP_011521616.1:n.124-653_124-645del
XM_011523315.3:c.124-653_124-645del	XP_011521617.1:n.124-653_124-645del
XM_011523316.3:c.124-653_124-645del	XP_011521618.1:n.124-653_124-645del
XM_017023654.2:c.124-653_124-645del	XP_016879143.1:n.124-653_124-645del
XM_017023655.2:c.124-653_124-645del	XP_016879144.1:n.124-653_124-645del
XM_017023656.2:c.124-653_124-645del	XP_016879145.1:n.124-653_124-645del
XM_017023657.2:c.124-653_124-645del	XP_016879146.1:n.124-653_124-645del
XM_017023658.2:c.124-653_124-645del	XP_016879147.1:n.124-653_124-645del
XM_024450437.1:c.124-653_124-645del	XP_024306205.1:n.124-653_124-645del
XR_002957840.1:n.167-653_167-645del
NM_001080432.3:c.124-653_124-645del MANE Select	NP_001073901.1:n.124-653_124-645del