Canonical Allele Identifier: CA1491646847
Gene: FAT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125434396T= , CM000666.2:g.125434396T= GRCh38
NC_000004.11:g.126355551T= , CM000666.1:g.126355551T= GRCh37
NC_000004.10:g.126575001T= NCBI36
NG_033865.1:g.122985T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394329.9:c.7170T= MANE Select ENSP00000377862.4:p.Asp2390=
ENST00000674496.2:c.1941T= ENSP00000501473.2:p.Asp647=
ENST00000335110.5:c.2064T= ENSP00000335169.5:p.Asp688=
ENST00000394329.7:c.7170T= ENSP00000377862.3:p.Asp2390=
NM_001291285.1:c.7170T= NP_001278214.1:p.Asp2390=
NM_001291303.1:c.7170T= NP_001278232.1:p.Asp2390=
NM_024582.4:c.7170T= NP_078858.4:p.Asp2390=
XM_011532236.1:c.7170T= XP_011530538.1:p.Asp2390=
XM_011532237.1:c.1941T= XP_011530539.1:p.Asp647=
XM_011532236.2:c.7170T= XP_011530538.1:p.Asp2390=
XM_011532237.2:c.1941T= XP_011530539.1:p.Asp647=
NM_001291285.2:c.7170T= NP_001278214.1:p.Asp2390=
NM_001291303.3:c.7170T= MANE Select NP_001278232.1:p.Asp2390=
NM_024582.5:c.7170T= NP_078858.4:p.Asp2390=
NM_001291285.3:c.7170T= NP_001278214.1:p.Asp2390=
NM_024582.6:c.7170T= NP_078858.4:p.Asp2390=