Canonical Allele Identifier: CA358117499
Gene: FAT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125317652T>A , CM000666.2:g.125317652T>A GRCh38
NC_000004.11:g.126238807T>A , CM000666.1:g.126238807T>A GRCh37
NC_000004.10:g.126458257T>A NCBI36
NG_033865.1:g.6241T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000394329.9:c.1241T>A MANE Select ENSP00000377862.4:p.Val414Glu
ENST00000674496.2:c.-55+1675T>A ENSP00000501473.2:n.-55+1675T>A
ENST00000394329.7:c.1241T>A ENSP00000377862.3:p.Val414Glu
NM_001291285.1:c.1241T>A NP_001278214.1:p.Val414Glu
NM_001291303.1:c.1241T>A NP_001278232.1:p.Val414Glu
NM_024582.4:c.1241T>A NP_078858.4:p.Val414Glu
XM_011532236.1:c.1241T>A XP_011530538.1:p.Val414Glu
XM_011532237.1:c.-55+1675T>A XP_011530539.1:n.-55+1675T>A
XM_011532236.2:c.1241T>A XP_011530538.1:p.Val414Glu
XM_011532237.2:c.-55+1675T>A XP_011530539.1:n.-55+1675T>A
NM_001291285.2:c.1241T>A NP_001278214.1:p.Val414Glu
NM_001291303.3:c.1241T>A MANE Select NP_001278232.1:p.Val414Glu
NM_024582.5:c.1241T>A NP_078858.4:p.Val414Glu
NM_001291285.3:c.1241T>A NP_001278214.1:p.Val414Glu
NM_024582.6:c.1241T>A NP_078858.4:p.Val414Glu