Canonical Allele Identifier: CA358143783

Gene: FAT4

Linked Data

• gnomAD v4: 4-125491649-T-G
• MyVariant Identifiers: chr4:g.126412804T>G (hg19) ; chr4:g.125491649T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491649T>G , CM000666.2:g.125491649T>G	GRCh38
NC_000004.11:g.126412804T>G , CM000666.1:g.126412804T>G	GRCh37
NC_000004.10:g.126632254T>G	NCBI36
NG_033865.1:g.180238T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14833T>G MANE Select	ENSP00000377862.4:p.Tyr4945Asp
ENST00000674496.2:c.9604T>G	ENSP00000501473.2:p.Tyr3202Asp
ENST00000335110.5:c.9550T>G	ENSP00000335169.5:p.Tyr3184Asp
ENST00000394329.7:c.14827T>G	ENSP00000377862.3:p.Tyr4943Asp
NM_001291285.1:c.14830T>G	NP_001278214.1:p.Tyr4944Asp
NM_001291303.1:c.14833T>G	NP_001278232.1:p.Tyr4945Asp
NM_024582.4:c.14827T>G	NP_078858.4:p.Tyr4943Asp
XM_011532236.1:c.14833T>G	XP_011530538.1:p.Tyr4945Asp
XM_011532237.1:c.9604T>G	XP_011530539.1:p.Tyr3202Asp
XM_011532236.2:c.14833T>G	XP_011530538.1:p.Tyr4945Asp
XM_011532237.2:c.9604T>G	XP_011530539.1:p.Tyr3202Asp
NM_001291285.2:c.14830T>G	NP_001278214.1:p.Tyr4944Asp
NM_001291303.3:c.14833T>G MANE Select	NP_001278232.1:p.Tyr4945Asp
NM_024582.5:c.14827T>G	NP_078858.4:p.Tyr4943Asp
NM_001291285.3:c.14830T>G	NP_001278214.1:p.Tyr4944Asp
NM_024582.6:c.14827T>G	NP_078858.4:p.Tyr4943Asp