Canonical Allele Identifier: CA2672009314
Gene: FAT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125318015_125318020del , CM000666.2:g.125318015_125318020del GRCh38
NC_000004.11:g.126239170_126239175del , CM000666.1:g.126239170_126239175del GRCh37
NC_000004.10:g.126458620_126458625del NCBI36
NG_033865.1:g.6604_6609del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394329.9:c.1604_1609del MANE Select ENSP00000377862.4:p.Gly535_Ser537delinsAla
ENST00000674496.2:c.-55+2038_-55+2043del ENSP00000501473.2:n.-55+2038_-55+2043del
ENST00000394329.7:c.1604_1609del ENSP00000377862.3:p.Gly535_Ser537delinsAla
NM_001291285.1:c.1604_1609del NP_001278214.1:p.Gly535_Ser537delinsAla
NM_001291303.1:c.1604_1609del NP_001278232.1:p.Gly535_Ser537delinsAla
NM_024582.4:c.1604_1609del NP_078858.4:p.Gly535_Ser537delinsAla
XM_011532236.1:c.1604_1609del XP_011530538.1:p.Gly535_Ser537delinsAla
XM_011532237.1:c.-55+2038_-55+2043del XP_011530539.1:n.-55+2038_-55+2043del
XM_011532236.2:c.1604_1609del XP_011530538.1:p.Gly535_Ser537delinsAla
XM_011532237.2:c.-55+2038_-55+2043del XP_011530539.1:n.-55+2038_-55+2043del
NM_001291285.2:c.1604_1609del NP_001278214.1:p.Gly535_Ser537delinsAla
NM_001291303.3:c.1604_1609del MANE Select NP_001278232.1:p.Gly535_Ser537delinsAla
NM_024582.5:c.1604_1609del NP_078858.4:p.Gly535_Ser537delinsAla
NM_001291285.3:c.1604_1609del NP_001278214.1:p.Gly535_Ser537delinsAla
NM_024582.6:c.1604_1609del NP_078858.4:p.Gly535_Ser537delinsAla