Canonical Allele Identifier: CA2572834861

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125317734_125317747del , CM000666.2:g.125317734_125317747del	GRCh38
NC_000004.11:g.126238889_126238902del , CM000666.1:g.126238889_126238902del	GRCh37
NC_000004.10:g.126458339_126458352del	NCBI36
NG_033865.1:g.6323_6336del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.1323_1336del MANE Select	ENSP00000377862.4:p.Asp442AlafsTer20
ENST00000674496.2:c.-55+1757_-55+1770del	ENSP00000501473.2:n.-55+1757_-55+1770del
ENST00000394329.7:c.1323_1336del	ENSP00000377862.3:p.Asp442AlafsTer20
NM_001291285.1:c.1323_1336del	NP_001278214.1:p.Asp442AlafsTer20
NM_001291303.1:c.1323_1336del	NP_001278232.1:p.Asp442AlafsTer20
NM_024582.4:c.1323_1336del	NP_078858.4:p.Asp442AlafsTer20
XM_011532236.1:c.1323_1336del	XP_011530538.1:p.Asp442AlafsTer20
XM_011532237.1:c.-55+1757_-55+1770del	XP_011530539.1:n.-55+1757_-55+1770del
XM_011532236.2:c.1323_1336del	XP_011530538.1:p.Asp442AlafsTer20
XM_011532237.2:c.-55+1757_-55+1770del	XP_011530539.1:n.-55+1757_-55+1770del
NM_001291285.2:c.1323_1336del	NP_001278214.1:p.Asp442AlafsTer20
NM_001291303.3:c.1323_1336del MANE Select	NP_001278232.1:p.Asp442AlafsTer20
NM_024582.5:c.1323_1336del	NP_078858.4:p.Asp442AlafsTer20
NM_001291285.3:c.1323_1336del	NP_001278214.1:p.Asp442AlafsTer20
NM_024582.6:c.1323_1336del	NP_078858.4:p.Asp442AlafsTer20