Canonical Allele Identifier: CA358120179
Gene: FAT4 HGNC NCBI

Linked Data

dbSNP Id: rs531595537

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125318783C>A , CM000666.2:g.125318783C>A GRCh38
NC_000004.11:g.126239938C>A , CM000666.1:g.126239938C>A GRCh37
NC_000004.10:g.126459388C>A NCBI36
NG_033865.1:g.7372C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394329.9:c.2372C>A MANE Select ENSP00000377862.4:p.Pro791His
ENST00000674496.2:c.-55+2806C>A ENSP00000501473.2:n.-55+2806C>A
ENST00000394329.7:c.2372C>A ENSP00000377862.3:p.Pro791His
NM_001291285.1:c.2372C>A NP_001278214.1:p.Pro791His
NM_001291303.1:c.2372C>A NP_001278232.1:p.Pro791His
NM_024582.4:c.2372C>A NP_078858.4:p.Pro791His
XM_011532236.1:c.2372C>A XP_011530538.1:p.Pro791His
XM_011532237.1:c.-55+2806C>A XP_011530539.1:n.-55+2806C>A
XM_011532236.2:c.2372C>A XP_011530538.1:p.Pro791His
XM_011532237.2:c.-55+2806C>A XP_011530539.1:n.-55+2806C>A
NM_001291285.2:c.2372C>A NP_001278214.1:p.Pro791His
NM_001291303.3:c.2372C>A MANE Select NP_001278232.1:p.Pro791His
NM_024582.5:c.2372C>A NP_078858.4:p.Pro791His
NM_001291285.3:c.2372C>A NP_001278214.1:p.Pro791His
NM_024582.6:c.2372C>A NP_078858.4:p.Pro791His