Canonical Allele Identifier: CA3480839

Gene: FCHSD1

Linked Data

• dbSNP Id: rs369917457
• ExAC: 5:141027016 G / T
• gnomAD v2: 5-141027016-G-T
• gnomAD v3: 5-141647449-G-T
• gnomAD v4: 5-141647449-G-T
• MyVariant Identifiers: chr5:g.141027016G>T (hg19) ; chr5:g.141647449G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647449G>T , CM000667.2:g.141647449G>T	GRCh38
NC_000005.9:g.141027016G>T , CM000667.1:g.141027016G>T	GRCh37
NC_000005.8:g.141007200G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.777C>A MANE Select	ENSP00000399259.2:p.Ala259=
ENST00000435817.6:c.777C>A	ENSP00000399259.2:p.Ala259=
ENST00000522126.5:c.549C>A	ENSP00000427796.1:p.Ala183=
ENST00000522386.1:n.383C>A
ENST00000522763.5:n.81C>A
ENST00000522783.5:c.771C>A	ENSP00000428677.1:p.Ala257=
ENST00000523856.5:n.35C>A
NM_033449.2:c.777C>A	NP_258260.1:p.Ala259=
XM_005268524.3:c.771C>A	XP_005268581.1:p.Ala257=
XM_006714803.2:c.648C>A	XP_006714866.1:p.Ala216=
XM_011537698.1:c.777C>A	XP_011536000.1:p.Ala259=
XM_011537699.1:c.777C>A	XP_011536001.1:p.Ala259=
XM_011537700.1:c.777C>A	XP_011536002.1:p.Ala259=
XM_011537701.1:c.777C>A	XP_011536003.1:p.Ala259=
XR_427781.2:n.831C>A
XR_944338.1:n.837C>A
XR_944339.1:n.837C>A
XM_005268524.5:c.771C>A	XP_005268581.1:p.Ala257=
XM_006714803.4:c.648C>A	XP_006714866.1:p.Ala216=
XM_011537698.3:c.777C>A	XP_011536000.1:p.Ala259=
XM_011537700.3:c.777C>A	XP_011536002.1:p.Ala259=
XM_011537701.3:c.777C>A	XP_011536003.1:p.Ala259=
XM_017010013.2:c.777C>A	XP_016865502.1:p.Ala259=
XR_002956197.1:n.773C>A
XR_427781.4:n.773C>A
XR_944338.3:n.852C>A
XR_944339.3:n.852C>A
NM_033449.3:c.777C>A MANE Select	NP_258260.1:p.Ala259=