Canonical Allele Identifier: CA1491680500

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491656_125491659delinsATGT , CM000666.2:g.125491656_125491659delinsATGT	GRCh38
NC_000004.11:g.126412811_126412814delinsATGT , CM000666.1:g.126412811_126412814delinsATGT	GRCh37
NC_000004.10:g.126632261_126632264delinsATGT	NCBI36
NG_033865.1:g.180245_180248delinsATGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14840_14843delinsATGT MANE Select	ENSP00000377862.4:p.Asp4947=
ENST00000674496.2:c.9611_9614delinsATGT	ENSP00000501473.2:p.Asp3204=
ENST00000335110.5:c.9557_9560delinsATGT	ENSP00000335169.5:p.Asp3186=
ENST00000394329.7:c.14834_14837delinsATGT	ENSP00000377862.3:p.Asp4945=
NM_001291285.1:c.14837_14840delinsATGT	NP_001278214.1:p.Asp4946=
NM_001291303.1:c.14840_14843delinsATGT	NP_001278232.1:p.Asp4947=
NM_024582.4:c.14834_14837delinsATGT	NP_078858.4:p.Asp4945=
XM_011532236.1:c.14840_14843delinsATGT	XP_011530538.1:p.Asp4947=
XM_011532237.1:c.9611_9614delinsATGT	XP_011530539.1:p.Asp3204=
XM_011532236.2:c.14840_14843delinsATGT	XP_011530538.1:p.Asp4947=
XM_011532237.2:c.9611_9614delinsATGT	XP_011530539.1:p.Asp3204=
NM_001291285.2:c.14837_14840delinsATGT	NP_001278214.1:p.Asp4946=
NM_001291303.3:c.14840_14843delinsATGT MANE Select	NP_001278232.1:p.Asp4947=
NM_024582.5:c.14834_14837delinsATGT	NP_078858.4:p.Asp4945=
NM_001291285.3:c.14837_14840delinsATGT	NP_001278214.1:p.Asp4946=
NM_024582.6:c.14834_14837delinsATGT	NP_078858.4:p.Asp4945=