Canonical Allele Identifier: CA3074398
Gene: FAT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125490421G>A , CM000666.2:g.125490421G>A GRCh38
NC_000004.11:g.126411576G>A , CM000666.1:g.126411576G>A GRCh37
NC_000004.10:g.126631026G>A NCBI36
NG_033865.1:g.179010G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394329.9:c.13605G>A MANE Select ENSP00000377862.4:p.Lys4535=
ENST00000674496.2:c.8376G>A ENSP00000501473.2:p.Lys2792=
ENST00000335110.5:c.8322G>A ENSP00000335169.5:p.Lys2774=
ENST00000394329.7:c.13599G>A ENSP00000377862.3:p.Lys4533=
NM_001291285.1:c.13602G>A NP_001278214.1:p.Lys4534=
NM_001291303.1:c.13605G>A NP_001278232.1:p.Lys4535=
NM_024582.4:c.13599G>A NP_078858.4:p.Lys4533=
XM_011532236.1:c.13605G>A XP_011530538.1:p.Lys4535=
XM_011532237.1:c.8376G>A XP_011530539.1:p.Lys2792=
XM_011532236.2:c.13605G>A XP_011530538.1:p.Lys4535=
XM_011532237.2:c.8376G>A XP_011530539.1:p.Lys2792=
NM_001291285.2:c.13602G>A NP_001278214.1:p.Lys4534=
NM_001291303.3:c.13605G>A MANE Select NP_001278232.1:p.Lys4535=
NM_024582.5:c.13599G>A NP_078858.4:p.Lys4533=
NM_001291285.3:c.13602G>A NP_001278214.1:p.Lys4534=
NM_024582.6:c.13599G>A NP_078858.4:p.Lys4533=