Canonical Allele Identifier: CA1491601219
Gene: FAT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125318008_125318017delinsACCACTGGGT , CM000666.2:g.125318008_125318017delinsACCACTGGGT GRCh38
NC_000004.11:g.126239163_126239172delinsACCACTGGGT , CM000666.1:g.126239163_126239172delinsACCACTGGGT GRCh37
NC_000004.10:g.126458613_126458622delinsACCACTGGGT NCBI36
NG_033865.1:g.6597_6606delinsACCACTGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394329.9:c.1597_1606delinsACCACTGGGT MANE Select ENSP00000377862.4:p.Thr533=
ENST00000674496.2:c.-55+2031_-55+2040delinsACCACTGGGT ENSP00000501473.2:n.-55+2031_-55+2040delinsACCACTGGGT
ENST00000394329.7:c.1597_1606delinsACCACTGGGT ENSP00000377862.3:p.Thr533=
NM_001291285.1:c.1597_1606delinsACCACTGGGT NP_001278214.1:p.Thr533=
NM_001291303.1:c.1597_1606delinsACCACTGGGT NP_001278232.1:p.Thr533=
NM_024582.4:c.1597_1606delinsACCACTGGGT NP_078858.4:p.Thr533=
XM_011532236.1:c.1597_1606delinsACCACTGGGT XP_011530538.1:p.Thr533=
XM_011532237.1:c.-55+2031_-55+2040delinsACCACTGGGT XP_011530539.1:n.-55+2031_-55+2040delinsACCACTGGGT
XM_011532236.2:c.1597_1606delinsACCACTGGGT XP_011530538.1:p.Thr533=
XM_011532237.2:c.-55+2031_-55+2040delinsACCACTGGGT XP_011530539.1:n.-55+2031_-55+2040delinsACCACTGGGT
NM_001291285.2:c.1597_1606delinsACCACTGGGT NP_001278214.1:p.Thr533=
NM_001291303.3:c.1597_1606delinsACCACTGGGT MANE Select NP_001278232.1:p.Thr533=
NM_024582.5:c.1597_1606delinsACCACTGGGT NP_078858.4:p.Thr533=
NM_001291285.3:c.1597_1606delinsACCACTGGGT NP_001278214.1:p.Thr533=
NM_024582.6:c.1597_1606delinsACCACTGGGT NP_078858.4:p.Thr533=