Canonical Allele Identifier: CA358143841

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126412817T>G (hg19) ; chr4:g.125491662T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491662T>G , CM000666.2:g.125491662T>G	GRCh38
NC_000004.11:g.126412817T>G , CM000666.1:g.126412817T>G	GRCh37
NC_000004.10:g.126632267T>G	NCBI36
NG_033865.1:g.180251T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14846T>G MANE Select	ENSP00000377862.4:p.Phe4949Cys
ENST00000674496.2:c.9617T>G	ENSP00000501473.2:p.Phe3206Cys
ENST00000335110.5:c.9563T>G	ENSP00000335169.5:p.Phe3188Cys
ENST00000394329.7:c.14840T>G	ENSP00000377862.3:p.Phe4947Cys
NM_001291285.1:c.14843T>G	NP_001278214.1:p.Phe4948Cys
NM_001291303.1:c.14846T>G	NP_001278232.1:p.Phe4949Cys
NM_024582.4:c.14840T>G	NP_078858.4:p.Phe4947Cys
XM_011532236.1:c.14846T>G	XP_011530538.1:p.Phe4949Cys
XM_011532237.1:c.9617T>G	XP_011530539.1:p.Phe3206Cys
XM_011532236.2:c.14846T>G	XP_011530538.1:p.Phe4949Cys
XM_011532237.2:c.9617T>G	XP_011530539.1:p.Phe3206Cys
NM_001291285.2:c.14843T>G	NP_001278214.1:p.Phe4948Cys
NM_001291303.3:c.14846T>G MANE Select	NP_001278232.1:p.Phe4949Cys
NM_024582.5:c.14840T>G	NP_078858.4:p.Phe4947Cys
NM_001291285.3:c.14843T>G	NP_001278214.1:p.Phe4948Cys
NM_024582.6:c.14840T>G	NP_078858.4:p.Phe4947Cys