Canonical Allele Identifier: CA446897247

Gene: FCHSD1

Linked Data

• MyVariant Identifiers: chr5:g.141026756A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647189A>C , CM000667.2:g.141647189A>C	GRCh38
NC_000005.9:g.141026756A>C , CM000667.1:g.141026756A>C	GRCh37
NC_000005.8:g.141006940A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.870T>G MANE Select	ENSP00000399259.2:p.Pro290=
ENST00000435817.6:c.870T>G	ENSP00000399259.2:p.Pro290=
ENST00000522126.5:c.642T>G	ENSP00000427796.1:p.Pro214=
ENST00000522386.1:n.476T>G
ENST00000522763.5:n.174T>G
ENST00000522783.5:c.864T>G	ENSP00000428677.1:p.Pro288=
ENST00000523856.5:n.128T>G
NM_033449.2:c.870T>G	NP_258260.1:p.Pro290=
XM_005268524.3:c.864T>G	XP_005268581.1:p.Pro288=
XM_006714803.2:c.741T>G	XP_006714866.1:p.Pro247=
XM_011537698.1:c.870T>G	XP_011536000.1:p.Pro290=
XM_011537699.1:c.870T>G	XP_011536001.1:p.Pro290=
XM_011537700.1:c.870T>G	XP_011536002.1:p.Pro290=
XM_011537701.1:c.870T>G	XP_011536003.1:p.Pro290=
XR_427781.2:n.924T>G
XR_944338.1:n.930T>G
XR_944339.1:n.930T>G
XM_005268524.5:c.864T>G	XP_005268581.1:p.Pro288=
XM_006714803.4:c.741T>G	XP_006714866.1:p.Pro247=
XM_011537698.3:c.870T>G	XP_011536000.1:p.Pro290=
XM_011537700.3:c.870T>G	XP_011536002.1:p.Pro290=
XM_011537701.3:c.870T>G	XP_011536003.1:p.Pro290=
XM_017010013.2:c.870T>G	XP_016865502.1:p.Pro290=
XR_002956197.1:n.866T>G
XR_427781.4:n.866T>G
XR_944338.3:n.945T>G
XR_944339.3:n.945T>G
NM_033449.3:c.870T>G MANE Select	NP_258260.1:p.Pro290=