Canonical Allele Identifier: CA358132487

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126402720T>A (hg19) ; chr4:g.125481565T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125481565T>A , CM000666.2:g.125481565T>A	GRCh38
NC_000004.11:g.126402720T>A , CM000666.1:g.126402720T>A	GRCh37
NC_000004.10:g.126622170T>A	NCBI36
NG_033865.1:g.170154T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.12649T>A MANE Select	ENSP00000377862.4:p.Leu4217Met
ENST00000674496.2:c.7420T>A	ENSP00000501473.2:p.Leu2474Met
ENST00000335110.5:c.7366T>A	ENSP00000335169.5:p.Leu2456Met
ENST00000394329.7:c.12643T>A	ENSP00000377862.3:p.Leu4215Met
NM_001291285.1:c.12649T>A	NP_001278214.1:p.Leu4217Met
NM_001291303.1:c.12649T>A	NP_001278232.1:p.Leu4217Met
NM_024582.4:c.12643T>A	NP_078858.4:p.Leu4215Met
XM_011532236.1:c.12649T>A	XP_011530538.1:p.Leu4217Met
XM_011532237.1:c.7420T>A	XP_011530539.1:p.Leu2474Met
XM_011532236.2:c.12649T>A	XP_011530538.1:p.Leu4217Met
XM_011532237.2:c.7420T>A	XP_011530539.1:p.Leu2474Met
NM_001291285.2:c.12649T>A	NP_001278214.1:p.Leu4217Met
NM_001291303.3:c.12649T>A MANE Select	NP_001278232.1:p.Leu4217Met
NM_024582.5:c.12643T>A	NP_078858.4:p.Leu4215Met
NM_001291285.3:c.12649T>A	NP_001278214.1:p.Leu4217Met
NM_024582.6:c.12643T>A	NP_078858.4:p.Leu4215Met