Canonical Allele Identifier: CA1491668599

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125481572A= , CM000666.2:g.125481572A=	GRCh38
NC_000004.11:g.126402727A= , CM000666.1:g.126402727A=	GRCh37
NC_000004.10:g.126622177A=	NCBI36
NG_033865.1:g.170161A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.12656A= MANE Select	ENSP00000377862.4:p.Tyr4219=
ENST00000674496.2:c.7427A=	ENSP00000501473.2:p.Tyr2476=
ENST00000335110.5:c.7373A=	ENSP00000335169.5:p.Tyr2458=
ENST00000394329.7:c.12650A=	ENSP00000377862.3:p.Tyr4217=
NM_001291285.1:c.12656A=	NP_001278214.1:p.Tyr4219=
NM_001291303.1:c.12656A=	NP_001278232.1:p.Tyr4219=
NM_024582.4:c.12650A=	NP_078858.4:p.Tyr4217=
XM_011532236.1:c.12656A=	XP_011530538.1:p.Tyr4219=
XM_011532237.1:c.7427A=	XP_011530539.1:p.Tyr2476=
XM_011532236.2:c.12656A=	XP_011530538.1:p.Tyr4219=
XM_011532237.2:c.7427A=	XP_011530539.1:p.Tyr2476=
NM_001291285.2:c.12656A=	NP_001278214.1:p.Tyr4219=
NM_001291303.3:c.12656A= MANE Select	NP_001278232.1:p.Tyr4219=
NM_024582.5:c.12650A=	NP_078858.4:p.Tyr4217=
NM_001291285.3:c.12656A=	NP_001278214.1:p.Tyr4219=
NM_024582.6:c.12650A=	NP_078858.4:p.Tyr4217=