Canonical Allele Identifier: CA3074629

Gene: FAT4

Linked Data

• dbSNP Id: rs758689576
• ExAC: 4:126412802 A / G
• gnomAD v2: 4-126412802-A-G
• gnomAD v4: 4-125491647-A-G
• MyVariant Identifiers: chr4:g.126412802A>G (hg19) ; chr4:g.125491647A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491647A>G , CM000666.2:g.125491647A>G	GRCh38
NC_000004.11:g.126412802A>G , CM000666.1:g.126412802A>G	GRCh37
NC_000004.10:g.126632252A>G	NCBI36
NG_033865.1:g.180236A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14831A>G MANE Select	ENSP00000377862.4:p.His4944Arg
ENST00000674496.2:c.9602A>G	ENSP00000501473.2:p.His3201Arg
ENST00000335110.5:c.9548A>G	ENSP00000335169.5:p.His3183Arg
ENST00000394329.7:c.14825A>G	ENSP00000377862.3:p.His4942Arg
NM_001291285.1:c.14828A>G	NP_001278214.1:p.His4943Arg
NM_001291303.1:c.14831A>G	NP_001278232.1:p.His4944Arg
NM_024582.4:c.14825A>G	NP_078858.4:p.His4942Arg
XM_011532236.1:c.14831A>G	XP_011530538.1:p.His4944Arg
XM_011532237.1:c.9602A>G	XP_011530539.1:p.His3201Arg
XM_011532236.2:c.14831A>G	XP_011530538.1:p.His4944Arg
XM_011532237.2:c.9602A>G	XP_011530539.1:p.His3201Arg
NM_001291285.2:c.14828A>G	NP_001278214.1:p.His4943Arg
NM_001291303.3:c.14831A>G MANE Select	NP_001278232.1:p.His4944Arg
NM_024582.5:c.14825A>G	NP_078858.4:p.His4942Arg
NM_001291285.3:c.14828A>G	NP_001278214.1:p.His4943Arg
NM_024582.6:c.14825A>G	NP_078858.4:p.His4942Arg