Canonical Allele Identifier: CA3073528

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125450461G>A , CM000666.2:g.125450461G>A	GRCh38
NC_000004.11:g.126371616G>A , CM000666.1:g.126371616G>A	GRCh37
NC_000004.10:g.126591066G>A	NCBI36
NG_033865.1:g.139050G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001291303.3:c.9451G>A MANE Select	NP_001278232.1:p.Ala3151Thr
ENST00000394329.9:c.9451G>A MANE Select	ENSP00000377862.4:p.Ala3151Thr
NM_001291285.1:c.9451G>A	NP_001278214.1:p.Ala3151Thr
NM_001291285.2:c.9451G>A	NP_001278214.1:p.Ala3151Thr
NM_001291285.3:c.9451G>A	NP_001278214.1:p.Ala3151Thr
NM_001291303.1:c.9451G>A	NP_001278232.1:p.Ala3151Thr
NM_024582.4:c.9445G>A	NP_078858.4:p.Ala3149Thr
NM_024582.5:c.9445G>A	NP_078858.4:p.Ala3149Thr
NM_024582.6:c.9445G>A	NP_078858.4:p.Ala3149Thr
ENST00000335110.5:c.4339G>A	ENSP00000335169.5:p.Ala1447Thr
ENST00000394329.7:c.9445G>A	ENSP00000377862.3:p.Ala3149Thr
ENST00000674496.2:c.4222G>A	ENSP00000501473.2:p.Ala1408Thr
XM_011532236.1:c.9451G>A	XP_011530538.1:p.Ala3151Thr
XM_011532236.2:c.9451G>A	XP_011530538.1:p.Ala3151Thr
XM_011532237.1:c.4222G>A	XP_011530539.1:p.Ala1408Thr
XM_011532237.2:c.4222G>A	XP_011530539.1:p.Ala1408Thr