Canonical Allele Identifier: CA1587311189

Gene: FCHSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141646913_141646915delinsCAG , CM000667.2:g.141646913_141646915delinsCAG	GRCh38
NC_000005.9:g.141026480_141026482delinsCAG , CM000667.1:g.141026480_141026482delinsCAG	GRCh37
NC_000005.8:g.141006664_141006666delinsCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.925-193_925-191delinsCTG MANE Select	ENSP00000399259.2:n.925-193_925-191delinsCTG
ENST00000435817.6:c.925-193_925-191delinsCTG	ENSP00000399259.2:n.925-193_925-191delinsCTG
ENST00000522126.5:c.697-193_697-191delinsCTG	ENSP00000427796.1:n.697-193_697-191delinsCTG
ENST00000522386.1:n.531-193_531-191delinsCTG
ENST00000522763.5:n.229-193_229-191delinsCTG
ENST00000522783.5:c.919-193_919-191delinsCTG	ENSP00000428677.1:n.919-193_919-191delinsCTG
ENST00000523856.5:n.183-193_183-191delinsCTG
NM_033449.2:c.925-193_925-191delinsCTG	NP_258260.1:n.925-193_925-191delinsCTG
XM_005268524.3:c.919-193_919-191delinsCTG	XP_005268581.1:n.919-193_919-191delinsCTG
XM_006714803.2:c.796-193_796-191delinsCTG	XP_006714866.1:n.796-193_796-191delinsCTG
XM_011537698.1:c.925-193_925-191delinsCTG	XP_011536000.1:n.925-193_925-191delinsCTG
XM_011537699.1:c.925-193_925-191delinsCTG	XP_011536001.1:n.925-193_925-191delinsCTG
XM_011537700.1:c.925-193_925-191delinsCTG	XP_011536002.1:n.925-193_925-191delinsCTG
XM_011537701.1:c.925-193_925-191delinsCTG	XP_011536003.1:n.925-193_925-191delinsCTG
XR_427781.2:n.979-193_979-191delinsCTG
XR_944338.1:n.985-193_985-191delinsCTG
XR_944339.1:n.985-193_985-191delinsCTG
XM_005268524.5:c.919-193_919-191delinsCTG	XP_005268581.1:n.919-193_919-191delinsCTG
XM_006714803.4:c.796-193_796-191delinsCTG	XP_006714866.1:n.796-193_796-191delinsCTG
XM_011537698.3:c.925-193_925-191delinsCTG	XP_011536000.1:n.925-193_925-191delinsCTG
XM_011537700.3:c.925-193_925-191delinsCTG	XP_011536002.1:n.925-193_925-191delinsCTG
XM_011537701.3:c.925-193_925-191delinsCTG	XP_011536003.1:n.925-193_925-191delinsCTG
XM_017010013.2:c.925-193_925-191delinsCTG	XP_016865502.1:n.925-193_925-191delinsCTG
XR_002956197.1:n.921-193_921-191delinsCTG
XR_427781.4:n.921-193_921-191delinsCTG
XR_944338.3:n.1000-193_1000-191delinsCTG
XR_944339.3:n.1000-193_1000-191delinsCTG
NM_033449.3:c.925-193_925-191delinsCTG MANE Select	NP_258260.1:n.925-193_925-191delinsCTG