Canonical Allele Identifier: CA1491662337

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125468636T= , CM000666.2:g.125468636T=	GRCh38
NC_000004.11:g.126389791T= , CM000666.1:g.126389791T=	GRCh37
NC_000004.10:g.126609241T=	NCBI36
NG_033865.1:g.157225T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.12030T= MANE Select	ENSP00000377862.4:p.His4010=
ENST00000674496.2:c.6801T=	ENSP00000501473.2:p.His2267=
ENST00000335110.5:c.6813T=	ENSP00000335169.5:p.His2271=
ENST00000394329.7:c.12024T=	ENSP00000377862.3:p.His4008=
NM_001291285.1:c.12030T=	NP_001278214.1:p.His4010=
NM_001291303.1:c.12030T=	NP_001278232.1:p.His4010=
NM_024582.4:c.12024T=	NP_078858.4:p.His4008=
XM_011532236.1:c.12030T=	XP_011530538.1:p.His4010=
XM_011532237.1:c.6801T=	XP_011530539.1:p.His2267=
XM_011532236.2:c.12030T=	XP_011530538.1:p.His4010=
XM_011532237.2:c.6801T=	XP_011530539.1:p.His2267=
NM_001291285.2:c.12030T=	NP_001278214.1:p.His4010=
NM_001291303.3:c.12030T= MANE Select	NP_001278232.1:p.His4010=
NM_024582.5:c.12024T=	NP_078858.4:p.His4008=
NM_001291285.3:c.12030T=	NP_001278214.1:p.His4010=
NM_024582.6:c.12024T=	NP_078858.4:p.His4008=