Canonical Allele Identifier: CA361562372
Gene: FCHSD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141647220T>C , CM000667.2:g.141647220T>C GRCh38
NC_000005.9:g.141026787T>C , CM000667.1:g.141026787T>C GRCh37
NC_000005.8:g.141006971T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435817.7:c.839A>G MANE Select ENSP00000399259.2:p.Glu280Gly
ENST00000435817.6:c.839A>G ENSP00000399259.2:p.Glu280Gly
ENST00000522126.5:c.611A>G ENSP00000427796.1:p.Glu204Gly
ENST00000522386.1:n.445A>G
ENST00000522763.5:n.143A>G
ENST00000522783.5:c.833A>G ENSP00000428677.1:p.Glu278Gly
ENST00000523856.5:n.97A>G
NM_033449.2:c.839A>G NP_258260.1:p.Glu280Gly
XM_005268524.3:c.833A>G XP_005268581.1:p.Glu278Gly
XM_006714803.2:c.710A>G XP_006714866.1:p.Glu237Gly
XM_011537698.1:c.839A>G XP_011536000.1:p.Glu280Gly
XM_011537699.1:c.839A>G XP_011536001.1:p.Glu280Gly
XM_011537700.1:c.839A>G XP_011536002.1:p.Glu280Gly
XM_011537701.1:c.839A>G XP_011536003.1:p.Glu280Gly
XR_427781.2:n.893A>G
XR_944338.1:n.899A>G
XR_944339.1:n.899A>G
XM_005268524.5:c.833A>G XP_005268581.1:p.Glu278Gly
XM_006714803.4:c.710A>G XP_006714866.1:p.Glu237Gly
XM_011537698.3:c.839A>G XP_011536000.1:p.Glu280Gly
XM_011537700.3:c.839A>G XP_011536002.1:p.Glu280Gly
XM_011537701.3:c.839A>G XP_011536003.1:p.Glu280Gly
XM_017010013.2:c.839A>G XP_016865502.1:p.Glu280Gly
XR_002956197.1:n.835A>G
XR_427781.4:n.835A>G
XR_944338.3:n.914A>G
XR_944339.3:n.914A>G
NM_033449.3:c.839A>G MANE Select NP_258260.1:p.Glu280Gly