Canonical Allele Identifier: CA1587311441
Gene: FCHSD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141647136T= , CM000667.2:g.141647136T= GRCh38
NC_000005.9:g.141026703T= , CM000667.1:g.141026703T= GRCh37
NC_000005.8:g.141006887T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435817.7:c.923A= MANE Select ENSP00000399259.2:p.Gln308=
ENST00000435817.6:c.923A= ENSP00000399259.2:p.Gln308=
ENST00000522126.5:c.695A= ENSP00000427796.1:p.Gln232=
ENST00000522386.1:n.529A=
ENST00000522763.5:n.227A=
ENST00000522783.5:c.917A= ENSP00000428677.1:p.Gln306=
ENST00000523856.5:n.181A=
NM_033449.2:c.923A= NP_258260.1:p.Gln308=
XM_005268524.3:c.917A= XP_005268581.1:p.Gln306=
XM_006714803.2:c.794A= XP_006714866.1:p.Gln265=
XM_011537698.1:c.923A= XP_011536000.1:p.Gln308=
XM_011537699.1:c.923A= XP_011536001.1:p.Gln308=
XM_011537700.1:c.923A= XP_011536002.1:p.Gln308=
XM_011537701.1:c.923A= XP_011536003.1:p.Gln308=
XR_427781.2:n.977A=
XR_944338.1:n.983A=
XR_944339.1:n.983A=
XM_005268524.5:c.917A= XP_005268581.1:p.Gln306=
XM_006714803.4:c.794A= XP_006714866.1:p.Gln265=
XM_011537698.3:c.923A= XP_011536000.1:p.Gln308=
XM_011537700.3:c.923A= XP_011536002.1:p.Gln308=
XM_011537701.3:c.923A= XP_011536003.1:p.Gln308=
XM_017010013.2:c.923A= XP_016865502.1:p.Gln308=
XR_002956197.1:n.919A=
XR_427781.4:n.919A=
XR_944338.3:n.998A=
XR_944339.3:n.998A=
NM_033449.3:c.923A= MANE Select NP_258260.1:p.Gln308=