Canonical Allele Identifier: CA1587311466

Gene: FCHSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647163T= , CM000667.2:g.141647163T=	GRCh38
NC_000005.9:g.141026730T= , CM000667.1:g.141026730T=	GRCh37
NC_000005.8:g.141006914T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.896A= MANE Select	ENSP00000399259.2:p.Gln299=
ENST00000435817.6:c.896A=	ENSP00000399259.2:p.Gln299=
ENST00000522126.5:c.668A=	ENSP00000427796.1:p.Gln223=
ENST00000522386.1:n.502A=
ENST00000522763.5:n.200A=
ENST00000522783.5:c.890A=	ENSP00000428677.1:p.Gln297=
ENST00000523856.5:n.154A=
NM_033449.2:c.896A=	NP_258260.1:p.Gln299=
XM_005268524.3:c.890A=	XP_005268581.1:p.Gln297=
XM_006714803.2:c.767A=	XP_006714866.1:p.Gln256=
XM_011537698.1:c.896A=	XP_011536000.1:p.Gln299=
XM_011537699.1:c.896A=	XP_011536001.1:p.Gln299=
XM_011537700.1:c.896A=	XP_011536002.1:p.Gln299=
XM_011537701.1:c.896A=	XP_011536003.1:p.Gln299=
XR_427781.2:n.950A=
XR_944338.1:n.956A=
XR_944339.1:n.956A=
XM_005268524.5:c.890A=	XP_005268581.1:p.Gln297=
XM_006714803.4:c.767A=	XP_006714866.1:p.Gln256=
XM_011537698.3:c.896A=	XP_011536000.1:p.Gln299=
XM_011537700.3:c.896A=	XP_011536002.1:p.Gln299=
XM_011537701.3:c.896A=	XP_011536003.1:p.Gln299=
XM_017010013.2:c.896A=	XP_016865502.1:p.Gln299=
XR_002956197.1:n.892A=
XR_427781.4:n.892A=
XR_944338.3:n.971A=
XR_944339.3:n.971A=
NM_033449.3:c.896A= MANE Select	NP_258260.1:p.Gln299=