Canonical Allele Identifier: CA1491600705

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125317757G= , CM000666.2:g.125317757G=	GRCh38
NC_000004.11:g.126238912G= , CM000666.1:g.126238912G=	GRCh37
NC_000004.10:g.126458362G=	NCBI36
NG_033865.1:g.6346G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.1346G= MANE Select	ENSP00000377862.4:p.Gly449=
ENST00000674496.2:c.-55+1780G=	ENSP00000501473.2:n.-55+1780G=
ENST00000394329.7:c.1346G=	ENSP00000377862.3:p.Gly449=
NM_001291285.1:c.1346G=	NP_001278214.1:p.Gly449=
NM_001291303.1:c.1346G=	NP_001278232.1:p.Gly449=
NM_024582.4:c.1346G=	NP_078858.4:p.Gly449=
XM_011532236.1:c.1346G=	XP_011530538.1:p.Gly449=
XM_011532237.1:c.-55+1780G=	XP_011530539.1:n.-55+1780G=
XM_011532236.2:c.1346G=	XP_011530538.1:p.Gly449=
XM_011532237.2:c.-55+1780G=	XP_011530539.1:n.-55+1780G=
NM_001291285.2:c.1346G=	NP_001278214.1:p.Gly449=
NM_001291303.3:c.1346G= MANE Select	NP_001278232.1:p.Gly449=
NM_024582.5:c.1346G=	NP_078858.4:p.Gly449=
NM_001291285.3:c.1346G=	NP_001278214.1:p.Gly449=
NM_024582.6:c.1346G=	NP_078858.4:p.Gly449=