Canonical Allele Identifier: CA358120712

Gene: FAT4

Linked Data

• ClinVar Variation Id: 2272892
• ClinVar RCV Id: RCV002799888 ; RCV003777795
• dbSNP Id: rs1296061836
• gnomAD v2: 4-126240180-A-G
• gnomAD v3: 4-125319025-A-G
• gnomAD v4: 4-125319025-A-G
• COSMIC: COSM5709031 ; COSM5709032
• MyVariant Identifiers: chr4:g.126240180A>G (hg19) ; chr4:g.125319025A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125319025A>G , CM000666.2:g.125319025A>G	GRCh38
NC_000004.11:g.126240180A>G , CM000666.1:g.126240180A>G	GRCh37
NC_000004.10:g.126459630A>G	NCBI36
NG_033865.1:g.7614A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.2614A>G MANE Select	ENSP00000377862.4:p.Thr872Ala
ENST00000674496.2:c.-55+3048A>G	ENSP00000501473.2:n.-55+3048A>G
ENST00000678072.1:n.220A>G
ENST00000394329.7:c.2614A>G	ENSP00000377862.3:p.Thr872Ala
NM_001291285.1:c.2614A>G	NP_001278214.1:p.Thr872Ala
NM_001291303.1:c.2614A>G	NP_001278232.1:p.Thr872Ala
NM_024582.4:c.2614A>G	NP_078858.4:p.Thr872Ala
XM_011532236.1:c.2614A>G	XP_011530538.1:p.Thr872Ala
XM_011532237.1:c.-55+3048A>G	XP_011530539.1:n.-55+3048A>G
XM_011532236.2:c.2614A>G	XP_011530538.1:p.Thr872Ala
XM_011532237.2:c.-55+3048A>G	XP_011530539.1:n.-55+3048A>G
NM_001291285.2:c.2614A>G	NP_001278214.1:p.Thr872Ala
NM_001291303.3:c.2614A>G MANE Select	NP_001278232.1:p.Thr872Ala
NM_024582.5:c.2614A>G	NP_078858.4:p.Thr872Ala
NM_001291285.3:c.2614A>G	NP_001278214.1:p.Thr872Ala
NM_024582.6:c.2614A>G	NP_078858.4:p.Thr872Ala