Canonical Allele Identifier: CA361564341
Gene: FCHSD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141647433C>T , CM000667.2:g.141647433C>T GRCh38
NC_000005.9:g.141027000C>T , CM000667.1:g.141027000C>T GRCh37
NC_000005.8:g.141007184C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435817.7:c.793G>A MANE Select ENSP00000399259.2:p.Glu265Lys
ENST00000435817.6:c.793G>A ENSP00000399259.2:p.Glu265Lys
ENST00000522126.5:c.565G>A ENSP00000427796.1:p.Glu189Lys
ENST00000522386.1:n.399G>A
ENST00000522763.5:n.97G>A
ENST00000522783.5:c.787G>A ENSP00000428677.1:p.Glu263Lys
ENST00000523856.5:n.51G>A
NM_033449.2:c.793G>A NP_258260.1:p.Glu265Lys
XM_005268524.3:c.787G>A XP_005268581.1:p.Glu263Lys
XM_006714803.2:c.664G>A XP_006714866.1:p.Glu222Lys
XM_011537698.1:c.793G>A XP_011536000.1:p.Glu265Lys
XM_011537699.1:c.793G>A XP_011536001.1:p.Glu265Lys
XM_011537700.1:c.793G>A XP_011536002.1:p.Glu265Lys
XM_011537701.1:c.793G>A XP_011536003.1:p.Glu265Lys
XR_427781.2:n.847G>A
XR_944338.1:n.853G>A
XR_944339.1:n.853G>A
XM_005268524.5:c.787G>A XP_005268581.1:p.Glu263Lys
XM_006714803.4:c.664G>A XP_006714866.1:p.Glu222Lys
XM_011537698.3:c.793G>A XP_011536000.1:p.Glu265Lys
XM_011537700.3:c.793G>A XP_011536002.1:p.Glu265Lys
XM_011537701.3:c.793G>A XP_011536003.1:p.Glu265Lys
XM_017010013.2:c.793G>A XP_016865502.1:p.Glu265Lys
XR_002956197.1:n.789G>A
XR_427781.4:n.789G>A
XR_944338.3:n.868G>A
XR_944339.3:n.868G>A
NM_033449.3:c.793G>A MANE Select NP_258260.1:p.Glu265Lys