Canonical Allele Identifier: CA3072124
Gene: FAT4 HGNC NCBI

Linked Data

dbSNP Id: rs775165068

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125318614C>T , CM000666.2:g.125318614C>T GRCh38
NC_000004.11:g.126239769C>T , CM000666.1:g.126239769C>T GRCh37
NC_000004.10:g.126459219C>T NCBI36
NG_033865.1:g.7203C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394329.9:c.2203C>T MANE Select ENSP00000377862.4:p.Arg735Trp
ENST00000674496.2:c.-55+2637C>T ENSP00000501473.2:n.-55+2637C>T
ENST00000394329.7:c.2203C>T ENSP00000377862.3:p.Arg735Trp
NM_001291285.1:c.2203C>T NP_001278214.1:p.Arg735Trp
NM_001291303.1:c.2203C>T NP_001278232.1:p.Arg735Trp
NM_024582.4:c.2203C>T NP_078858.4:p.Arg735Trp
XM_011532236.1:c.2203C>T XP_011530538.1:p.Arg735Trp
XM_011532237.1:c.-55+2637C>T XP_011530539.1:n.-55+2637C>T
XM_011532236.2:c.2203C>T XP_011530538.1:p.Arg735Trp
XM_011532237.2:c.-55+2637C>T XP_011530539.1:n.-55+2637C>T
NM_001291285.2:c.2203C>T NP_001278214.1:p.Arg735Trp
NM_001291303.3:c.2203C>T MANE Select NP_001278232.1:p.Arg735Trp
NM_024582.5:c.2203C>T NP_078858.4:p.Arg735Trp
NM_001291285.3:c.2203C>T NP_001278214.1:p.Arg735Trp
NM_024582.6:c.2203C>T NP_078858.4:p.Arg735Trp