Canonical Allele Identifier: CA3073297

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125449018A>G , CM000666.2:g.125449018A>G	GRCh38
NC_000004.11:g.126370173A>G , CM000666.1:g.126370173A>G	GRCh37
NC_000004.10:g.126589623A>G	NCBI36
NG_033865.1:g.137607A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001291303.3:c.8008A>G MANE Select	NP_001278232.1:p.Ile2670Val
ENST00000394329.9:c.8008A>G MANE Select	ENSP00000377862.4:p.Ile2670Val
NM_001291285.1:c.8008A>G	NP_001278214.1:p.Ile2670Val
NM_001291285.2:c.8008A>G	NP_001278214.1:p.Ile2670Val
NM_001291285.3:c.8008A>G	NP_001278214.1:p.Ile2670Val
NM_001291303.1:c.8008A>G	NP_001278232.1:p.Ile2670Val
NM_024582.4:c.8002A>G	NP_078858.4:p.Ile2668Val
NM_024582.5:c.8002A>G	NP_078858.4:p.Ile2668Val
NM_024582.6:c.8002A>G	NP_078858.4:p.Ile2668Val
ENST00000335110.5:c.2896A>G	ENSP00000335169.5:p.Ile966Val
ENST00000394329.7:c.8002A>G	ENSP00000377862.3:p.Ile2668Val
ENST00000674496.2:c.2779A>G	ENSP00000501473.2:p.Ile927Val
XM_011532236.1:c.8008A>G	XP_011530538.1:p.Ile2670Val
XM_011532236.2:c.8008A>G	XP_011530538.1:p.Ile2670Val
XM_011532237.1:c.2779A>G	XP_011530539.1:p.Ile927Val
XM_011532237.2:c.2779A>G	XP_011530539.1:p.Ile927Val