Canonical Allele Identifier: CA6227089

Gene: FAT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92798190A>G , CM000673.2:g.92798190A>G	GRCh38
NC_000011.9:g.92531356A>G , CM000673.1:g.92531356A>G	GRCh37
NC_000011.8:g.92171004A>G	NCBI36
NG_052813.1:g.578555A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001367949.2:c.5177A>G MANE Select	NP_001354878.1:p.Gln1726Arg
ENST00000525166.6:c.5177A>G MANE Select	ENSP00000432586.2:p.Gln1726Arg
NM_001008781.2:c.5177A>G	NP_001008781.2:p.Gln1726Arg
NM_001008781.3:c.5177A>G	NP_001008781.2:p.Gln1726Arg
NM_001367949.1:c.5177A>G	NP_001354878.1:p.Gln1726Arg
ENST00000409404.6:c.5177A>G	ENSP00000387040.2:p.Gln1726Arg
ENST00000525166.5:c.4727A>G	ENSP00000432586.1:p.Gln1576Arg
XM_011542584.1:c.5291A>G	XP_011540886.1:p.Gln1764Arg
XM_017017178.2:c.5246A>G	XP_016872667.1:p.Gln1749Arg
XM_017017179.2:c.5246A>G	XP_016872668.1:p.Gln1749Arg
XM_017017180.1:c.5246A>G	XP_016872669.1:p.Gln1749Arg
XM_017017181.2:c.5177A>G	XP_016872670.1:p.Gln1726Arg
XM_017017182.2:c.5246A>G	XP_016872671.1:p.Gln1749Arg
XM_017017183.2:c.5177A>G	XP_016872672.1:p.Gln1726Arg
XM_017017184.2:c.5246A>G	XP_016872673.1:p.Gln1749Arg
XM_017017185.1:c.2030A>G	XP_016872674.1:p.Gln677Arg
XM_017017186.1:c.1916A>G	XP_016872675.1:p.Gln639Arg
XM_017017187.1:c.1916A>G	XP_016872676.1:p.Gln639Arg