Canonical Allele Identifier: CA1587311954

Gene: FCHSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647419G= , CM000667.2:g.141647419G=	GRCh38
NC_000005.9:g.141026986G= , CM000667.1:g.141026986G=	GRCh37
NC_000005.8:g.141007170G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.807C= MANE Select	ENSP00000399259.2:p.Arg269=
ENST00000435817.6:c.807C=	ENSP00000399259.2:p.Arg269=
ENST00000522126.5:c.579C=	ENSP00000427796.1:p.Arg193=
ENST00000522386.1:n.413C=
ENST00000522763.5:n.111C=
ENST00000522783.5:c.801C=	ENSP00000428677.1:p.Arg267=
ENST00000523856.5:n.65C=
NM_033449.2:c.807C=	NP_258260.1:p.Arg269=
XM_005268524.3:c.801C=	XP_005268581.1:p.Arg267=
XM_006714803.2:c.678C=	XP_006714866.1:p.Arg226=
XM_011537698.1:c.807C=	XP_011536000.1:p.Arg269=
XM_011537699.1:c.807C=	XP_011536001.1:p.Arg269=
XM_011537700.1:c.807C=	XP_011536002.1:p.Arg269=
XM_011537701.1:c.807C=	XP_011536003.1:p.Arg269=
XR_427781.2:n.861C=
XR_944338.1:n.867C=
XR_944339.1:n.867C=
XM_005268524.5:c.801C=	XP_005268581.1:p.Arg267=
XM_006714803.4:c.678C=	XP_006714866.1:p.Arg226=
XM_011537698.3:c.807C=	XP_011536000.1:p.Arg269=
XM_011537700.3:c.807C=	XP_011536002.1:p.Arg269=
XM_011537701.3:c.807C=	XP_011536003.1:p.Arg269=
XM_017010013.2:c.807C=	XP_016865502.1:p.Arg269=
XR_002956197.1:n.803C=
XR_427781.4:n.803C=
XR_944338.3:n.882C=
XR_944339.3:n.882C=
NM_033449.3:c.807C= MANE Select	NP_258260.1:p.Arg269=