Canonical Allele Identifier: CA441373844

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126412800C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491645C>G , CM000666.2:g.125491645C>G	GRCh38
NC_000004.11:g.126412800C>G , CM000666.1:g.126412800C>G	GRCh37
NC_000004.10:g.126632250C>G	NCBI36
NG_033865.1:g.180234C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14829C>G MANE Select	ENSP00000377862.4:p.Gly4943=
ENST00000674496.2:c.9600C>G	ENSP00000501473.2:p.Gly3200=
ENST00000335110.5:c.9546C>G	ENSP00000335169.5:p.Gly3182=
ENST00000394329.7:c.14823C>G	ENSP00000377862.3:p.Gly4941=
NM_001291285.1:c.14826C>G	NP_001278214.1:p.Gly4942=
NM_001291303.1:c.14829C>G	NP_001278232.1:p.Gly4943=
NM_024582.4:c.14823C>G	NP_078858.4:p.Gly4941=
XM_011532236.1:c.14829C>G	XP_011530538.1:p.Gly4943=
XM_011532237.1:c.9600C>G	XP_011530539.1:p.Gly3200=
XM_011532236.2:c.14829C>G	XP_011530538.1:p.Gly4943=
XM_011532237.2:c.9600C>G	XP_011530539.1:p.Gly3200=
NM_001291285.2:c.14826C>G	NP_001278214.1:p.Gly4942=
NM_001291303.3:c.14829C>G MANE Select	NP_001278232.1:p.Gly4943=
NM_024582.5:c.14823C>G	NP_078858.4:p.Gly4941=
NM_001291285.3:c.14826C>G	NP_001278214.1:p.Gly4942=
NM_024582.6:c.14823C>G	NP_078858.4:p.Gly4941=