Canonical Allele Identifier: CA3073580

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125450810A>G , CM000666.2:g.125450810A>G	GRCh38
NC_000004.11:g.126371965A>G , CM000666.1:g.126371965A>G	GRCh37
NC_000004.10:g.126591415A>G	NCBI36
NG_033865.1:g.139399A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.9800A>G MANE Select	ENSP00000377862.4:p.His3267Arg
ENST00000674496.2:c.4571A>G	ENSP00000501473.2:p.His1524Arg
ENST00000335110.5:c.4688A>G	ENSP00000335169.5:p.His1563Arg
ENST00000394329.7:c.9794A>G	ENSP00000377862.3:p.His3265Arg
NM_001291285.1:c.9800A>G	NP_001278214.1:p.His3267Arg
NM_001291303.1:c.9800A>G	NP_001278232.1:p.His3267Arg
NM_024582.4:c.9794A>G	NP_078858.4:p.His3265Arg
XM_011532236.1:c.9800A>G	XP_011530538.1:p.His3267Arg
XM_011532237.1:c.4571A>G	XP_011530539.1:p.His1524Arg
XM_011532236.2:c.9800A>G	XP_011530538.1:p.His3267Arg
XM_011532237.2:c.4571A>G	XP_011530539.1:p.His1524Arg
NM_001291285.2:c.9800A>G	NP_001278214.1:p.His3267Arg
NM_001291303.3:c.9800A>G MANE Select	NP_001278232.1:p.His3267Arg
NM_024582.5:c.9794A>G	NP_078858.4:p.His3265Arg
NM_001291285.3:c.9800A>G	NP_001278214.1:p.His3267Arg
NM_024582.6:c.9794A>G	NP_078858.4:p.His3265Arg