Canonical Allele Identifier: CA1587311692

Gene: FCHSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647272A= , CM000667.2:g.141647272A=	GRCh38
NC_000005.9:g.141026839A= , CM000667.1:g.141026839A=	GRCh37
NC_000005.8:g.141007023A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.829-42T= MANE Select	ENSP00000399259.2:n.829-42T=
ENST00000435817.6:c.829-42T=	ENSP00000399259.2:n.829-42T=
ENST00000522126.5:c.601-42T=	ENSP00000427796.1:n.601-42T=
ENST00000522386.1:n.435-42T=
ENST00000522763.5:n.133-42T=
ENST00000522783.5:c.823-42T=	ENSP00000428677.1:n.823-42T=
ENST00000523856.5:n.87-42T=
NM_033449.2:c.829-42T=	NP_258260.1:n.829-42T=
XM_005268524.3:c.823-42T=	XP_005268581.1:n.823-42T=
XM_006714803.2:c.700-42T=	XP_006714866.1:n.700-42T=
XM_011537698.1:c.829-42T=	XP_011536000.1:n.829-42T=
XM_011537699.1:c.829-42T=	XP_011536001.1:n.829-42T=
XM_011537700.1:c.829-42T=	XP_011536002.1:n.829-42T=
XM_011537701.1:c.829-42T=	XP_011536003.1:n.829-42T=
XR_427781.2:n.883-42T=
XR_944338.1:n.889-42T=
XR_944339.1:n.889-42T=
XM_005268524.5:c.823-42T=	XP_005268581.1:n.823-42T=
XM_006714803.4:c.700-42T=	XP_006714866.1:n.700-42T=
XM_011537698.3:c.829-42T=	XP_011536000.1:n.829-42T=
XM_011537700.3:c.829-42T=	XP_011536002.1:n.829-42T=
XM_011537701.3:c.829-42T=	XP_011536003.1:n.829-42T=
XM_017010013.2:c.829-42T=	XP_016865502.1:n.829-42T=
XR_002956197.1:n.825-42T=
XR_427781.4:n.825-42T=
XR_944338.3:n.904-42T=
XR_944339.3:n.904-42T=
NM_033449.3:c.829-42T= MANE Select	NP_258260.1:n.829-42T=