Canonical Allele Identifier: CA1491680481
Gene: FAT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125491647A= , CM000666.2:g.125491647A= GRCh38
NC_000004.11:g.126412802A= , CM000666.1:g.126412802A= GRCh37
NC_000004.10:g.126632252A= NCBI36
NG_033865.1:g.180236A=

Transcript Alleles

HGVS Amino-acid change
ENST00000394329.9:c.14831A= MANE Select ENSP00000377862.4:p.His4944=
ENST00000674496.2:c.9602A= ENSP00000501473.2:p.His3201=
ENST00000335110.5:c.9548A= ENSP00000335169.5:p.His3183=
ENST00000394329.7:c.14825A= ENSP00000377862.3:p.His4942=
NM_001291285.1:c.14828A= NP_001278214.1:p.His4943=
NM_001291303.1:c.14831A= NP_001278232.1:p.His4944=
NM_024582.4:c.14825A= NP_078858.4:p.His4942=
XM_011532236.1:c.14831A= XP_011530538.1:p.His4944=
XM_011532237.1:c.9602A= XP_011530539.1:p.His3201=
XM_011532236.2:c.14831A= XP_011530538.1:p.His4944=
XM_011532237.2:c.9602A= XP_011530539.1:p.His3201=
NM_001291285.2:c.14828A= NP_001278214.1:p.His4943=
NM_001291303.3:c.14831A= MANE Select NP_001278232.1:p.His4944=
NM_024582.5:c.14825A= NP_078858.4:p.His4942=
NM_001291285.3:c.14828A= NP_001278214.1:p.His4943=
NM_024582.6:c.14825A= NP_078858.4:p.His4942=