Canonical Allele Identifier: CA3480799

Gene: FCHSD1

Linked Data

• dbSNP Id: rs773582412
• ExAC: 5:141026703 T / C
• gnomAD v2: 5-141026703-T-C
• gnomAD v4: 5-141647136-T-C
• MyVariant Identifiers: chr5:g.141026703T>C (hg19) ; chr5:g.141647136T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.923A>G MANE Select	ENSP00000399259.2:p.Gln308Arg
ENST00000435817.6:c.923A>G	ENSP00000399259.2:p.Gln308Arg
ENST00000522126.5:c.695A>G	ENSP00000427796.1:p.Gln232Arg
ENST00000522386.1:n.529A>G
ENST00000522763.5:n.227A>G
ENST00000522783.5:c.917A>G	ENSP00000428677.1:p.Gln306Arg
ENST00000523856.5:n.181A>G
NM_033449.2:c.923A>G	NP_258260.1:p.Gln308Arg
XM_005268524.3:c.917A>G	XP_005268581.1:p.Gln306Arg
XM_006714803.2:c.794A>G	XP_006714866.1:p.Gln265Arg
XM_011537698.1:c.923A>G	XP_011536000.1:p.Gln308Arg
XM_011537699.1:c.923A>G	XP_011536001.1:p.Gln308Arg
XM_011537700.1:c.923A>G	XP_011536002.1:p.Gln308Arg
XM_011537701.1:c.923A>G	XP_011536003.1:p.Gln308Arg
XR_427781.2:n.977A>G
XR_944338.1:n.983A>G
XR_944339.1:n.983A>G
XM_005268524.5:c.917A>G	XP_005268581.1:p.Gln306Arg
XM_006714803.4:c.794A>G	XP_006714866.1:p.Gln265Arg
XM_011537698.3:c.923A>G	XP_011536000.1:p.Gln308Arg
XM_011537700.3:c.923A>G	XP_011536002.1:p.Gln308Arg
XM_011537701.3:c.923A>G	XP_011536003.1:p.Gln308Arg
XM_017010013.2:c.923A>G	XP_016865502.1:p.Gln308Arg
XR_002956197.1:n.919A>G
XR_427781.4:n.919A>G
XR_944338.3:n.998A>G
XR_944339.3:n.998A>G
NM_033449.3:c.923A>G MANE Select	NP_258260.1:p.Gln308Arg