Canonical Allele Identifier: CA2571095342

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125468691del , CM000666.2:g.125468691del	GRCh38
NC_000004.11:g.126389846del , CM000666.1:g.126389846del	GRCh37
NC_000004.10:g.126609296del	NCBI36
NG_033865.1:g.157280del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.12085del MANE Select	ENSP00000377862.4:p.Ala4029ProfsTer9
ENST00000674496.2:c.6856del	ENSP00000501473.2:p.Ala2286ProfsTer9
ENST00000335110.5:c.6868del	ENSP00000335169.5:p.Ala2290ProfsTer9
ENST00000394329.7:c.12079del	ENSP00000377862.3:p.Ala4027ProfsTer9
NM_001291285.1:c.12085del	NP_001278214.1:p.Ala4029ProfsTer9
NM_001291303.1:c.12085del	NP_001278232.1:p.Ala4029ProfsTer9
NM_024582.4:c.12079del	NP_078858.4:p.Ala4027ProfsTer9
XM_011532236.1:c.12085del	XP_011530538.1:p.Ala4029ProfsTer9
XM_011532237.1:c.6856del	XP_011530539.1:p.Ala2286ProfsTer9
XM_011532236.2:c.12085del	XP_011530538.1:p.Ala4029ProfsTer9
XM_011532237.2:c.6856del	XP_011530539.1:p.Ala2286ProfsTer9
NM_001291285.2:c.12085del	NP_001278214.1:p.Ala4029ProfsTer9
NM_001291303.3:c.12085del MANE Select	NP_001278232.1:p.Ala4029ProfsTer9
NM_024582.5:c.12079del	NP_078858.4:p.Ala4027ProfsTer9
NM_001291285.3:c.12085del	NP_001278214.1:p.Ala4029ProfsTer9
NM_024582.6:c.12079del	NP_078858.4:p.Ala4027ProfsTer9