Canonical Allele Identifier: CA441204969

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126355407T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125434252T>G , CM000666.2:g.125434252T>G	GRCh38
NC_000004.11:g.126355407T>G , CM000666.1:g.126355407T>G	GRCh37
NC_000004.10:g.126574857T>G	NCBI36
NG_033865.1:g.122841T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.7026T>G MANE Select	ENSP00000377862.4:p.Pro2342=
ENST00000674496.2:c.1797T>G	ENSP00000501473.2:p.Pro599=
ENST00000335110.5:c.1920T>G	ENSP00000335169.5:p.Pro640=
ENST00000394329.7:c.7026T>G	ENSP00000377862.3:p.Pro2342=
NM_001291285.1:c.7026T>G	NP_001278214.1:p.Pro2342=
NM_001291303.1:c.7026T>G	NP_001278232.1:p.Pro2342=
NM_024582.4:c.7026T>G	NP_078858.4:p.Pro2342=
XM_011532236.1:c.7026T>G	XP_011530538.1:p.Pro2342=
XM_011532237.1:c.1797T>G	XP_011530539.1:p.Pro599=
XM_011532236.2:c.7026T>G	XP_011530538.1:p.Pro2342=
XM_011532237.2:c.1797T>G	XP_011530539.1:p.Pro599=
NM_001291285.2:c.7026T>G	NP_001278214.1:p.Pro2342=
NM_001291303.3:c.7026T>G MANE Select	NP_001278232.1:p.Pro2342=
NM_024582.5:c.7026T>G	NP_078858.4:p.Pro2342=
NM_001291285.3:c.7026T>G	NP_001278214.1:p.Pro2342=
NM_024582.6:c.7026T>G	NP_078858.4:p.Pro2342=