Canonical Allele Identifier: CA441366367

Gene: FAT4

Linked Data

• gnomAD v4: 4-125317467-A-G
• MyVariant Identifiers: chr4:g.126238622A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125317467A>G , CM000666.2:g.125317467A>G	GRCh38
NC_000004.11:g.126238622A>G , CM000666.1:g.126238622A>G	GRCh37
NC_000004.10:g.126458072A>G	NCBI36
NG_033865.1:g.6056A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.1056A>G MANE Select	ENSP00000377862.4:p.Val352=
ENST00000674496.2:c.-55+1490A>G	ENSP00000501473.2:n.-55+1490A>G
ENST00000394329.7:c.1056A>G	ENSP00000377862.3:p.Val352=
NM_001291285.1:c.1056A>G	NP_001278214.1:p.Val352=
NM_001291303.1:c.1056A>G	NP_001278232.1:p.Val352=
NM_024582.4:c.1056A>G	NP_078858.4:p.Val352=
XM_011532236.1:c.1056A>G	XP_011530538.1:p.Val352=
XM_011532237.1:c.-55+1490A>G	XP_011530539.1:n.-55+1490A>G
XM_011532236.2:c.1056A>G	XP_011530538.1:p.Val352=
XM_011532237.2:c.-55+1490A>G	XP_011530539.1:n.-55+1490A>G
NM_001291285.2:c.1056A>G	NP_001278214.1:p.Val352=
NM_001291303.3:c.1056A>G MANE Select	NP_001278232.1:p.Val352=
NM_024582.5:c.1056A>G	NP_078858.4:p.Val352=
NM_001291285.3:c.1056A>G	NP_001278214.1:p.Val352=
NM_024582.6:c.1056A>G	NP_078858.4:p.Val352=