Canonical Allele Identifier: CA1491662418

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125468837A= , CM000666.2:g.125468837A=	GRCh38
NC_000004.11:g.126389992A= , CM000666.1:g.126389992A=	GRCh37
NC_000004.10:g.126609442A=	NCBI36
NG_033865.1:g.157426A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.12213+18A= MANE Select	ENSP00000377862.4:n.12213+18A=
ENST00000674496.2:c.6984+18A=	ENSP00000501473.2:n.6984+18A=
ENST00000335110.5:c.6996+18A=	ENSP00000335169.5:n.6996+18A=
ENST00000394329.7:c.12207+18A=	ENSP00000377862.3:n.12207+18A=
NM_001291285.1:c.12213+18A=	NP_001278214.1:n.12213+18A=
NM_001291303.1:c.12213+18A=	NP_001278232.1:n.12213+18A=
NM_024582.4:c.12207+18A=	NP_078858.4:n.12207+18A=
XM_011532236.1:c.12213+18A=	XP_011530538.1:n.12213+18A=
XM_011532237.1:c.6984+18A=	XP_011530539.1:n.6984+18A=
XM_011532236.2:c.12213+18A=	XP_011530538.1:n.12213+18A=
XM_011532237.2:c.6984+18A=	XP_011530539.1:n.6984+18A=
NM_001291285.2:c.12213+18A=	NP_001278214.1:n.12213+18A=
NM_001291303.3:c.12213+18A= MANE Select	NP_001278232.1:n.12213+18A=
NM_024582.5:c.12207+18A=	NP_078858.4:n.12207+18A=
NM_001291285.3:c.12213+18A=	NP_001278214.1:n.12213+18A=
NM_024582.6:c.12207+18A=	NP_078858.4:n.12207+18A=