Canonical Allele Identifier: CA1587311918

Gene: FCHSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647407T= , CM000667.2:g.141647407T=	GRCh38
NC_000005.9:g.141026974T= , CM000667.1:g.141026974T=	GRCh37
NC_000005.8:g.141007158T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.819A= MANE Select	ENSP00000399259.2:p.Thr273=
ENST00000435817.6:c.819A=	ENSP00000399259.2:p.Thr273=
ENST00000522126.5:c.591A=	ENSP00000427796.1:p.Thr197=
ENST00000522386.1:n.425A=
ENST00000522763.5:n.123A=
ENST00000522783.5:c.813A=	ENSP00000428677.1:p.Thr271=
ENST00000523856.5:n.77A=
NM_033449.2:c.819A=	NP_258260.1:p.Thr273=
XM_005268524.3:c.813A=	XP_005268581.1:p.Thr271=
XM_006714803.2:c.690A=	XP_006714866.1:p.Thr230=
XM_011537698.1:c.819A=	XP_011536000.1:p.Thr273=
XM_011537699.1:c.819A=	XP_011536001.1:p.Thr273=
XM_011537700.1:c.819A=	XP_011536002.1:p.Thr273=
XM_011537701.1:c.819A=	XP_011536003.1:p.Thr273=
XR_427781.2:n.873A=
XR_944338.1:n.879A=
XR_944339.1:n.879A=
XM_005268524.5:c.813A=	XP_005268581.1:p.Thr271=
XM_006714803.4:c.690A=	XP_006714866.1:p.Thr230=
XM_011537698.3:c.819A=	XP_011536000.1:p.Thr273=
XM_011537700.3:c.819A=	XP_011536002.1:p.Thr273=
XM_011537701.3:c.819A=	XP_011536003.1:p.Thr273=
XM_017010013.2:c.819A=	XP_016865502.1:p.Thr273=
XR_002956197.1:n.815A=
XR_427781.4:n.815A=
XR_944338.3:n.894A=
XR_944339.3:n.894A=
NM_033449.3:c.819A= MANE Select	NP_258260.1:p.Thr273=