Canonical Allele Identifier: CA358143768

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126412799G>T (hg19) ; chr4:g.125491644G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491644G>T , CM000666.2:g.125491644G>T	GRCh38
NC_000004.11:g.126412799G>T , CM000666.1:g.126412799G>T	GRCh37
NC_000004.10:g.126632249G>T	NCBI36
NG_033865.1:g.180233G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14828G>T MANE Select	ENSP00000377862.4:p.Gly4943Val
ENST00000674496.2:c.9599G>T	ENSP00000501473.2:p.Gly3200Val
ENST00000335110.5:c.9545G>T	ENSP00000335169.5:p.Gly3182Val
ENST00000394329.7:c.14822G>T	ENSP00000377862.3:p.Gly4941Val
NM_001291285.1:c.14825G>T	NP_001278214.1:p.Gly4942Val
NM_001291303.1:c.14828G>T	NP_001278232.1:p.Gly4943Val
NM_024582.4:c.14822G>T	NP_078858.4:p.Gly4941Val
XM_011532236.1:c.14828G>T	XP_011530538.1:p.Gly4943Val
XM_011532237.1:c.9599G>T	XP_011530539.1:p.Gly3200Val
XM_011532236.2:c.14828G>T	XP_011530538.1:p.Gly4943Val
XM_011532237.2:c.9599G>T	XP_011530539.1:p.Gly3200Val
NM_001291285.2:c.14825G>T	NP_001278214.1:p.Gly4942Val
NM_001291303.3:c.14828G>T MANE Select	NP_001278232.1:p.Gly4943Val
NM_024582.5:c.14822G>T	NP_078858.4:p.Gly4941Val
NM_001291285.3:c.14825G>T	NP_001278214.1:p.Gly4942Val
NM_024582.6:c.14822G>T	NP_078858.4:p.Gly4941Val