Canonical Allele Identifier: CA622576058

Gene: FTO

Linked Data

• dbSNP Id: rs1464235534
• gnomAD v2: 16-54027980-CCT-C
• gnomAD v3: 16-53994068-CCT-C
• gnomAD v4: 16-53994068-CCT-C
• MyVariant Identifiers: chr16:g.54027981_54027982del (hg19) ; chr16:g.53994069_53994070del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53994073_53994074del , CM000678.2:g.53994073_53994074del	GRCh38
NC_000016.9:g.54027985_54027986del , CM000678.1:g.54027985_54027986del	GRCh37
NC_000016.8:g.52585486_52585487del	NCBI36
NG_012969.1:g.295111_295112del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471389.6:c.1364+59964_1364+59965del MANE Select	ENSP00000418823.1:n.1364+59964_1364+59965del
ENST00000563011.2:c.745-45272_745-45271del
ENST00000612285.2:c.389+59964_389+59965del	ENSP00000490300.1:n.389+59964_389+59965del
ENST00000635892.1:n.214+59964_214+59965del
ENST00000636491.1:c.1347-14355_1347-14354del	ENSP00000490047.1:n.1347-14355_1347-14354del
ENST00000636992.1:c.1240-19305_1240-19304del	ENSP00000489886.1:n.1240-19305_1240-19304del
ENST00000637562.1:c.1364+59964_1364+59965del	ENSP00000490426.1:n.1364+59964_1364+59965del
ENST00000637845.1:c.1364+59964_1364+59965del	ENSP00000489638.1:n.1364+59964_1364+59965del
ENST00000637969.1:c.1364+59964_1364+59965del	ENSP00000490516.1:n.1364+59964_1364+59965del
ENST00000268349.7:c.97+9119_97+9120del	ENSP00000268349.7:n.97+9119_97+9120del
ENST00000431610.6:c.167+59964_167+59965del	ENSP00000415636.2:n.167+59964_167+59965del
ENST00000460382.5:c.167+59964_167+59965del	ENSP00000417422.1:n.167+59964_167+59965del
ENST00000463855.1:c.230+59964_230+59965del	ENSP00000417843.1:n.230+59964_230+59965del
ENST00000464071.1:c.*523+59964_*523+59965del	ENSP00000418424.1:n.*523+59964_*523+59965del
ENST00000471389.5:c.1364+59964_1364+59965del	ENSP00000418823.1:n.1364+59964_1364+59965del
NM_001080432.2:c.1364+59964_1364+59965del	NP_001073901.1:n.1364+59964_1364+59965del
XM_011523313.1:c.1394+59964_1394+59965del	XP_011521615.1:n.1394+59964_1394+59965del
XM_011523316.1:c.1395-14355_1395-14354del	XP_011521618.1:n.1395-14355_1395-14354del
NM_001363891.1:c.1394+59964_1394+59965del	NP_001350820.1:n.1394+59964_1394+59965del
NM_001363894.1:c.1427+59964_1427+59965del	NP_001350823.1:n.1427+59964_1427+59965del
NM_001363896.1:c.1346+37284_1346+37285del	NP_001350825.1:n.1346+37284_1346+37285del
NM_001363897.1:c.1286+59964_1286+59965del	NP_001350826.1:n.1286+59964_1286+59965del
NM_001363898.1:c.1250+59964_1250+59965del	NP_001350827.1:n.1250+59964_1250+59965del
NM_001363899.1:c.1250+59964_1250+59965del	NP_001350828.1:n.1250+59964_1250+59965del
NM_001363900.1:c.1220+59964_1220+59965del	NP_001350829.1:n.1220+59964_1220+59965del
NM_001363901.1:c.1220+59964_1220+59965del	NP_001350830.1:n.1220+59964_1220+59965del
NM_001363903.1:c.1239+105122_1239+105123del	NP_001350832.1:n.1239+105122_1239+105123del
NM_001363905.1:c.851+59964_851+59965del	NP_001350834.1:n.851+59964_851+59965del
NM_001363988.1:c.*22+37284_*22+37285del	NP_001350917.1:n.*22+37284_*22+37285del
NR_156761.1:n.614+59964_614+59965del
XM_011523316.3:c.1395-14355_1395-14354del	XP_011521618.1:n.1395-14355_1395-14354del
XM_024450437.1:c.1365-14355_1365-14354del	XP_024306205.1:n.1365-14355_1365-14354del
NM_001080432.3:c.1364+59964_1364+59965del MANE Select	NP_001073901.1:n.1364+59964_1364+59965del