Canonical Allele Identifier: CA358135226
Gene: FAT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125434329C>G , CM000666.2:g.125434329C>G GRCh38
NC_000004.11:g.126355484C>G , CM000666.1:g.126355484C>G GRCh37
NC_000004.10:g.126574934C>G NCBI36
NG_033865.1:g.122918C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000394329.9:c.7103C>G MANE Select ENSP00000377862.4:p.Ala2368Gly
ENST00000674496.2:c.1874C>G ENSP00000501473.2:p.Ala625Gly
ENST00000335110.5:c.1997C>G ENSP00000335169.5:p.Ala666Gly
ENST00000394329.7:c.7103C>G ENSP00000377862.3:p.Ala2368Gly
NM_001291285.1:c.7103C>G NP_001278214.1:p.Ala2368Gly
NM_001291303.1:c.7103C>G NP_001278232.1:p.Ala2368Gly
NM_024582.4:c.7103C>G NP_078858.4:p.Ala2368Gly
XM_011532236.1:c.7103C>G XP_011530538.1:p.Ala2368Gly
XM_011532237.1:c.1874C>G XP_011530539.1:p.Ala625Gly
XM_011532236.2:c.7103C>G XP_011530538.1:p.Ala2368Gly
XM_011532237.2:c.1874C>G XP_011530539.1:p.Ala625Gly
NM_001291285.2:c.7103C>G NP_001278214.1:p.Ala2368Gly
NM_001291303.3:c.7103C>G MANE Select NP_001278232.1:p.Ala2368Gly
NM_024582.5:c.7103C>G NP_078858.4:p.Ala2368Gly
NM_001291285.3:c.7103C>G NP_001278214.1:p.Ala2368Gly
NM_024582.6:c.7103C>G NP_078858.4:p.Ala2368Gly