Canonical Allele Identifier: CA14220227
Gene: FTO HGNC NCBI

Linked Data

dbSNP Id: rs16953002

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.54080912G>A , CM000678.2:g.54080912G>A GRCh38
NC_000016.9:g.54114824G>A , CM000678.1:g.54114824G>A GRCh37
NC_000016.8:g.52672325G>A NCBI36
NG_012969.1:g.381950G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000471389.6:c.1365-30850G>A MANE Select ENSP00000418823.1:p.=
ENST00000612285.2:n.390-30850G>A ENSP00000490300.1:p.=
ENST00000635892.1:n.215-30850G>A
ENST00000636091.1:n.2645+8372G>A
ENST00000636992.1:c.*108-30850G>A ENSP00000489886.1:p.=
ENST00000637562.1:c.*55+19192G>A ENSP00000490426.1:p.=
ENST00000637845.1:c.1365-30850G>A ENSP00000489638.1:p.=
ENST00000637969.1:c.1365-30850G>A ENSP00000490516.1:p.=
ENST00000268349.7:n.98-30850G>A ENSP00000268349.7:p.=
ENST00000431610.6:c.168-30850G>A ENSP00000415636.2:p.=
ENST00000460382.5:c.168-30850G>A ENSP00000417422.1:p.=
ENST00000463855.1:c.231-30850G>A ENSP00000417843.1:p.=
ENST00000464071.1:c.*524-30850G>A ENSP00000418424.1:p.=
ENST00000471389.5:c.1365-30850G>A ENSP00000418823.1:p.=
ENST00000472835.1:n.306+16970G>A
NM_001080432.2:c.1365-30850G>A NP_001073901.1:p.=
XM_011523313.1:c.1395-30850G>A XP_011521615.1:p.=
NM_001363891.1:c.1395-30850G>A NP_001350820.1:p.=
NM_001363894.1:c.1428-30850G>A NP_001350823.1:p.=
NM_001363896.1:c.1347-30850G>A NP_001350825.1:p.=
NM_001363897.1:c.1287-30850G>A NP_001350826.1:p.=
NM_001363898.1:c.1251-30850G>A NP_001350827.1:p.=
NM_001363899.1:c.1251-30850G>A NP_001350828.1:p.=
NM_001363900.1:c.1221-30850G>A NP_001350829.1:p.=
NM_001363901.1:c.1221-30850G>A NP_001350830.1:p.=
NM_001363903.1:c.1240-30850G>A NP_001350832.1:p.=
NM_001363905.1:c.852-30850G>A NP_001350834.1:p.=
NM_001363988.1:c.*23-30850G>A NP_001350917.1:p.=
NR_156761.1:n.615-30850G>A
NM_001080432.3:c.1365-30850G>A MANE Select NP_001073901.1:p.=