Canonical Allele Identifier: CA1587311287
Gene: FCHSD1 HGNC NCBI

Linked Data

dbSNP Id: rs2099907745

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141646978_141646979insAC , CM000667.2:g.141646978_141646979insAC GRCh38
NC_000005.9:g.141026545_141026546insAC , CM000667.1:g.141026545_141026546insAC GRCh37
NC_000005.8:g.141006729_141006730insAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435817.7:c.924+156_924+157insGT MANE Select ENSP00000399259.2:n.924+156_924+157insGT
ENST00000435817.6:c.924+156_924+157insGT ENSP00000399259.2:n.924+156_924+157insGT
ENST00000522126.5:c.696+156_696+157insGT ENSP00000427796.1:n.696+156_696+157insGT
ENST00000522386.1:n.530+156_530+157insGT
ENST00000522763.5:n.228+156_228+157insGT
ENST00000522783.5:c.918+156_918+157insGT ENSP00000428677.1:n.918+156_918+157insGT
ENST00000523856.5:n.182+156_182+157insGT
NM_033449.2:c.924+156_924+157insGT NP_258260.1:n.924+156_924+157insGT
XM_005268524.3:c.918+156_918+157insGT XP_005268581.1:n.918+156_918+157insGT
XM_006714803.2:c.795+156_795+157insGT XP_006714866.1:n.795+156_795+157insGT
XM_011537698.1:c.924+156_924+157insGT XP_011536000.1:n.924+156_924+157insGT
XM_011537699.1:c.924+156_924+157insGT XP_011536001.1:n.924+156_924+157insGT
XM_011537700.1:c.924+156_924+157insGT XP_011536002.1:n.924+156_924+157insGT
XM_011537701.1:c.924+156_924+157insGT XP_011536003.1:n.924+156_924+157insGT
XR_427781.2:n.978+156_978+157insGT
XR_944338.1:n.984+156_984+157insGT
XR_944339.1:n.984+156_984+157insGT
XM_005268524.5:c.918+156_918+157insGT XP_005268581.1:n.918+156_918+157insGT
XM_006714803.4:c.795+156_795+157insGT XP_006714866.1:n.795+156_795+157insGT
XM_011537698.3:c.924+156_924+157insGT XP_011536000.1:n.924+156_924+157insGT
XM_011537700.3:c.924+156_924+157insGT XP_011536002.1:n.924+156_924+157insGT
XM_011537701.3:c.924+156_924+157insGT XP_011536003.1:n.924+156_924+157insGT
XM_017010013.2:c.924+156_924+157insGT XP_016865502.1:n.924+156_924+157insGT
XR_002956197.1:n.920+156_920+157insGT
XR_427781.4:n.920+156_920+157insGT
XR_944338.3:n.999+156_999+157insGT
XR_944339.3:n.999+156_999+157insGT
NM_033449.3:c.924+156_924+157insGT MANE Select NP_258260.1:n.924+156_924+157insGT