Canonical Allele Identifier: CA358135368

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126355528G>T (hg19) ; chr4:g.125434373G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125434373G>T , CM000666.2:g.125434373G>T	GRCh38
NC_000004.11:g.126355528G>T , CM000666.1:g.126355528G>T	GRCh37
NC_000004.10:g.126574978G>T	NCBI36
NG_033865.1:g.122962G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.7147G>T MANE Select	ENSP00000377862.4:p.Val2383Phe
ENST00000674496.2:c.1918G>T	ENSP00000501473.2:p.Val640Phe
ENST00000335110.5:c.2041G>T	ENSP00000335169.5:p.Val681Phe
ENST00000394329.7:c.7147G>T	ENSP00000377862.3:p.Val2383Phe
NM_001291285.1:c.7147G>T	NP_001278214.1:p.Val2383Phe
NM_001291303.1:c.7147G>T	NP_001278232.1:p.Val2383Phe
NM_024582.4:c.7147G>T	NP_078858.4:p.Val2383Phe
XM_011532236.1:c.7147G>T	XP_011530538.1:p.Val2383Phe
XM_011532237.1:c.1918G>T	XP_011530539.1:p.Val640Phe
XM_011532236.2:c.7147G>T	XP_011530538.1:p.Val2383Phe
XM_011532237.2:c.1918G>T	XP_011530539.1:p.Val640Phe
NM_001291285.2:c.7147G>T	NP_001278214.1:p.Val2383Phe
NM_001291303.3:c.7147G>T MANE Select	NP_001278232.1:p.Val2383Phe
NM_024582.5:c.7147G>T	NP_078858.4:p.Val2383Phe
NM_001291285.3:c.7147G>T	NP_001278214.1:p.Val2383Phe
NM_024582.6:c.7147G>T	NP_078858.4:p.Val2383Phe