Canonical Allele Identifier: CA1491680483
Gene: FAT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125491648T= , CM000666.2:g.125491648T= GRCh38
NC_000004.11:g.126412803T= , CM000666.1:g.126412803T= GRCh37
NC_000004.10:g.126632253T= NCBI36
NG_033865.1:g.180237T=

Transcript Alleles

HGVS Amino-acid change
ENST00000394329.9:c.14832T= MANE Select ENSP00000377862.4:p.His4944=
ENST00000674496.2:c.9603T= ENSP00000501473.2:p.His3201=
ENST00000335110.5:c.9549T= ENSP00000335169.5:p.His3183=
ENST00000394329.7:c.14826T= ENSP00000377862.3:p.His4942=
NM_001291285.1:c.14829T= NP_001278214.1:p.His4943=
NM_001291303.1:c.14832T= NP_001278232.1:p.His4944=
NM_024582.4:c.14826T= NP_078858.4:p.His4942=
XM_011532236.1:c.14832T= XP_011530538.1:p.His4944=
XM_011532237.1:c.9603T= XP_011530539.1:p.His3201=
XM_011532236.2:c.14832T= XP_011530538.1:p.His4944=
XM_011532237.2:c.9603T= XP_011530539.1:p.His3201=
NM_001291285.2:c.14829T= NP_001278214.1:p.His4943=
NM_001291303.3:c.14832T= MANE Select NP_001278232.1:p.His4944=
NM_024582.5:c.14826T= NP_078858.4:p.His4942=
NM_001291285.3:c.14829T= NP_001278214.1:p.His4943=
NM_024582.6:c.14826T= NP_078858.4:p.His4942=