Canonical Allele Identifier: CA3074157

Gene: FAT4

Linked Data

• dbSNP Id: rs771271104
• ExAC: 4:126402635 A / G
• gnomAD v2: 4-126402635-A-G
• gnomAD v3: 4-125481480-A-G
• gnomAD v4: 4-125481480-A-G
• MyVariant Identifiers: chr4:g.126402635A>G (hg19) ; chr4:g.125481480A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125481480A>G , CM000666.2:g.125481480A>G	GRCh38
NC_000004.11:g.126402635A>G , CM000666.1:g.126402635A>G	GRCh37
NC_000004.10:g.126622085A>G	NCBI36
NG_033865.1:g.170069A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.12605-41A>G MANE Select	ENSP00000377862.4:n.12605-41A>G
ENST00000674496.2:c.7376-41A>G	ENSP00000501473.2:n.7376-41A>G
ENST00000335110.5:c.7322-41A>G	ENSP00000335169.5:n.7322-41A>G
ENST00000394329.7:c.12599-41A>G	ENSP00000377862.3:n.12599-41A>G
NM_001291285.1:c.12605-41A>G	NP_001278214.1:n.12605-41A>G
NM_001291303.1:c.12605-41A>G	NP_001278232.1:n.12605-41A>G
NM_024582.4:c.12599-41A>G	NP_078858.4:n.12599-41A>G
XM_011532236.1:c.12605-41A>G	XP_011530538.1:n.12605-41A>G
XM_011532237.1:c.7376-41A>G	XP_011530539.1:n.7376-41A>G
XM_011532236.2:c.12605-41A>G	XP_011530538.1:n.12605-41A>G
XM_011532237.2:c.7376-41A>G	XP_011530539.1:n.7376-41A>G
NM_001291285.2:c.12605-41A>G	NP_001278214.1:n.12605-41A>G
NM_001291303.3:c.12605-41A>G MANE Select	NP_001278232.1:n.12605-41A>G
NM_024582.5:c.12599-41A>G	NP_078858.4:n.12599-41A>G
NM_001291285.3:c.12605-41A>G	NP_001278214.1:n.12605-41A>G
NM_024582.6:c.12599-41A>G	NP_078858.4:n.12599-41A>G