Canonical Allele Identifier: CA358127865

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126389766T>A (hg19) ; chr4:g.125468611T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125468611T>A , CM000666.2:g.125468611T>A	GRCh38
NC_000004.11:g.126389766T>A , CM000666.1:g.126389766T>A	GRCh37
NC_000004.10:g.126609216T>A	NCBI36
NG_033865.1:g.157200T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.12005T>A MANE Select	ENSP00000377862.4:p.Val4002Asp
ENST00000674496.2:c.6776T>A	ENSP00000501473.2:p.Val2259Asp
ENST00000335110.5:c.6788T>A	ENSP00000335169.5:p.Val2263Asp
ENST00000394329.7:c.11999T>A	ENSP00000377862.3:p.Val4000Asp
NM_001291285.1:c.12005T>A	NP_001278214.1:p.Val4002Asp
NM_001291303.1:c.12005T>A	NP_001278232.1:p.Val4002Asp
NM_024582.4:c.11999T>A	NP_078858.4:p.Val4000Asp
XM_011532236.1:c.12005T>A	XP_011530538.1:p.Val4002Asp
XM_011532237.1:c.6776T>A	XP_011530539.1:p.Val2259Asp
XM_011532236.2:c.12005T>A	XP_011530538.1:p.Val4002Asp
XM_011532237.2:c.6776T>A	XP_011530539.1:p.Val2259Asp
NM_001291285.2:c.12005T>A	NP_001278214.1:p.Val4002Asp
NM_001291303.3:c.12005T>A MANE Select	NP_001278232.1:p.Val4002Asp
NM_024582.5:c.11999T>A	NP_078858.4:p.Val4000Asp
NM_001291285.3:c.12005T>A	NP_001278214.1:p.Val4002Asp
NM_024582.6:c.11999T>A	NP_078858.4:p.Val4000Asp