Canonical Allele Identifier: CA3073141

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125446324A>T , CM000666.2:g.125446324A>T	GRCh38
NC_000004.11:g.126367479A>T , CM000666.1:g.126367479A>T	GRCh37
NC_000004.10:g.126586929A>T	NCBI36
NG_033865.1:g.134913A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001291303.3:c.7231A>T MANE Select	NP_001278232.1:p.Thr2411Ser
ENST00000394329.9:c.7231A>T MANE Select	ENSP00000377862.4:p.Thr2411Ser
NM_001291285.1:c.7231A>T	NP_001278214.1:p.Thr2411Ser
NM_001291285.2:c.7231A>T	NP_001278214.1:p.Thr2411Ser
NM_001291285.3:c.7231A>T	NP_001278214.1:p.Thr2411Ser
NM_001291303.1:c.7231A>T	NP_001278232.1:p.Thr2411Ser
NM_024582.4:c.7225A>T	NP_078858.4:p.Thr2409Ser
NM_024582.5:c.7225A>T	NP_078858.4:p.Thr2409Ser
NM_024582.6:c.7225A>T	NP_078858.4:p.Thr2409Ser
ENST00000335110.5:c.2119A>T	ENSP00000335169.5:p.Thr707Ser
ENST00000394329.7:c.7225A>T	ENSP00000377862.3:p.Thr2409Ser
ENST00000509444.1:n.214A>T
ENST00000674496.2:c.2002A>T	ENSP00000501473.2:p.Thr668Ser
XM_011532236.1:c.7231A>T	XP_011530538.1:p.Thr2411Ser
XM_011532236.2:c.7231A>T	XP_011530538.1:p.Thr2411Ser
XM_011532237.1:c.2002A>T	XP_011530539.1:p.Thr668Ser
XM_011532237.2:c.2002A>T	XP_011530539.1:p.Thr668Ser