Canonical Allele Identifier: CA361564271

Gene: FCHSD1

Linked Data

• gnomAD v4: 5-141647427-C-T
• MyVariant Identifiers: chr5:g.141026994C>T (hg19) ; chr5:g.141647427C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647427C>T , CM000667.2:g.141647427C>T	GRCh38
NC_000005.9:g.141026994C>T , CM000667.1:g.141026994C>T	GRCh37
NC_000005.8:g.141007178C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.799G>A MANE Select	ENSP00000399259.2:p.Ala267Thr
ENST00000435817.6:c.799G>A	ENSP00000399259.2:p.Ala267Thr
ENST00000522126.5:c.571G>A	ENSP00000427796.1:p.Ala191Thr
ENST00000522386.1:n.405G>A
ENST00000522763.5:n.103G>A
ENST00000522783.5:c.793G>A	ENSP00000428677.1:p.Ala265Thr
ENST00000523856.5:n.57G>A
NM_033449.2:c.799G>A	NP_258260.1:p.Ala267Thr
XM_005268524.3:c.793G>A	XP_005268581.1:p.Ala265Thr
XM_006714803.2:c.670G>A	XP_006714866.1:p.Ala224Thr
XM_011537698.1:c.799G>A	XP_011536000.1:p.Ala267Thr
XM_011537699.1:c.799G>A	XP_011536001.1:p.Ala267Thr
XM_011537700.1:c.799G>A	XP_011536002.1:p.Ala267Thr
XM_011537701.1:c.799G>A	XP_011536003.1:p.Ala267Thr
XR_427781.2:n.853G>A
XR_944338.1:n.859G>A
XR_944339.1:n.859G>A
XM_005268524.5:c.793G>A	XP_005268581.1:p.Ala265Thr
XM_006714803.4:c.670G>A	XP_006714866.1:p.Ala224Thr
XM_011537698.3:c.799G>A	XP_011536000.1:p.Ala267Thr
XM_011537700.3:c.799G>A	XP_011536002.1:p.Ala267Thr
XM_011537701.3:c.799G>A	XP_011536003.1:p.Ala267Thr
XM_017010013.2:c.799G>A	XP_016865502.1:p.Ala267Thr
XR_002956197.1:n.795G>A
XR_427781.4:n.795G>A
XR_944338.3:n.874G>A
XR_944339.3:n.874G>A
NM_033449.3:c.799G>A MANE Select	NP_258260.1:p.Ala267Thr