Canonical Allele Identifier: CA1587311609

Gene: FCHSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647225_141647226delinsGC , CM000667.2:g.141647225_141647226delinsGC	GRCh38
NC_000005.9:g.141026792_141026793delinsGC , CM000667.1:g.141026792_141026793delinsGC	GRCh37
NC_000005.8:g.141006976_141006977delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.833_834delinsGC MANE Select	ENSP00000399259.2:p.Ser278=
ENST00000435817.6:c.833_834delinsGC	ENSP00000399259.2:p.Ser278=
ENST00000522126.5:c.605_606delinsGC	ENSP00000427796.1:p.Ser202=
ENST00000522386.1:n.439_440delinsGC
ENST00000522763.5:n.137_138delinsGC
ENST00000522783.5:c.827_828delinsGC	ENSP00000428677.1:p.Ser276=
ENST00000523856.5:n.91_92delinsGC
NM_033449.2:c.833_834delinsGC	NP_258260.1:p.Ser278=
XM_005268524.3:c.827_828delinsGC	XP_005268581.1:p.Ser276=
XM_006714803.2:c.704_705delinsGC	XP_006714866.1:p.Ser235=
XM_011537698.1:c.833_834delinsGC	XP_011536000.1:p.Ser278=
XM_011537699.1:c.833_834delinsGC	XP_011536001.1:p.Ser278=
XM_011537700.1:c.833_834delinsGC	XP_011536002.1:p.Ser278=
XM_011537701.1:c.833_834delinsGC	XP_011536003.1:p.Ser278=
XR_427781.2:n.887_888delinsGC
XR_944338.1:n.893_894delinsGC
XR_944339.1:n.893_894delinsGC
XM_005268524.5:c.827_828delinsGC	XP_005268581.1:p.Ser276=
XM_006714803.4:c.704_705delinsGC	XP_006714866.1:p.Ser235=
XM_011537698.3:c.833_834delinsGC	XP_011536000.1:p.Ser278=
XM_011537700.3:c.833_834delinsGC	XP_011536002.1:p.Ser278=
XM_011537701.3:c.833_834delinsGC	XP_011536003.1:p.Ser278=
XM_017010013.2:c.833_834delinsGC	XP_016865502.1:p.Ser278=
XR_002956197.1:n.829_830delinsGC
XR_427781.4:n.829_830delinsGC
XR_944338.3:n.908_909delinsGC
XR_944339.3:n.908_909delinsGC
NM_033449.3:c.833_834delinsGC MANE Select	NP_258260.1:p.Ser278=