Canonical Allele Identifier: CA3073774

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125452049C>T , CM000666.2:g.125452049C>T	GRCh38
NC_000004.11:g.126373204C>T , CM000666.1:g.126373204C>T	GRCh37
NC_000004.10:g.126592654C>T	NCBI36
NG_033865.1:g.140638C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001291303.3:c.11039C>T MANE Select	NP_001278232.1:p.Thr3680Met
ENST00000394329.9:c.11039C>T MANE Select	ENSP00000377862.4:p.Thr3680Met
NM_001291285.1:c.11039C>T	NP_001278214.1:p.Thr3680Met
NM_001291285.2:c.11039C>T	NP_001278214.1:p.Thr3680Met
NM_001291285.3:c.11039C>T	NP_001278214.1:p.Thr3680Met
NM_001291303.1:c.11039C>T	NP_001278232.1:p.Thr3680Met
NM_024582.4:c.11033C>T	NP_078858.4:p.Thr3678Met
NM_024582.5:c.11033C>T	NP_078858.4:p.Thr3678Met
NM_024582.6:c.11033C>T	NP_078858.4:p.Thr3678Met
ENST00000335110.5:c.5927C>T	ENSP00000335169.5:p.Thr1976Met
ENST00000394329.7:c.11033C>T	ENSP00000377862.3:p.Thr3678Met
ENST00000674496.2:c.5810C>T	ENSP00000501473.2:p.Thr1937Met
XM_011532236.1:c.11039C>T	XP_011530538.1:p.Thr3680Met
XM_011532236.2:c.11039C>T	XP_011530538.1:p.Thr3680Met
XM_011532237.1:c.5810C>T	XP_011530539.1:p.Thr1937Met
XM_011532237.2:c.5810C>T	XP_011530539.1:p.Thr1937Met