Canonical Allele Identifier: CA446897335

Gene: FCHSD1

Linked Data

• MyVariant Identifiers: chr5:g.141027043G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647476G>C , CM000667.2:g.141647476G>C	GRCh38
NC_000005.9:g.141027043G>C , CM000667.1:g.141027043G>C	GRCh37
NC_000005.8:g.141007227G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.750C>G MANE Select	ENSP00000399259.2:p.Thr250=
ENST00000435817.6:c.750C>G	ENSP00000399259.2:p.Thr250=
ENST00000522126.5:c.522C>G	ENSP00000427796.1:p.Thr174=
ENST00000522386.1:n.356C>G
ENST00000522763.5:n.54C>G
ENST00000522783.5:c.744C>G	ENSP00000428677.1:p.Thr248=
ENST00000523856.5:n.8C>G
NM_033449.2:c.750C>G	NP_258260.1:p.Thr250=
XM_005268524.3:c.744C>G	XP_005268581.1:p.Thr248=
XM_006714803.2:c.621C>G	XP_006714866.1:p.Thr207=
XM_011537698.1:c.750C>G	XP_011536000.1:p.Thr250=
XM_011537699.1:c.750C>G	XP_011536001.1:p.Thr250=
XM_011537700.1:c.750C>G	XP_011536002.1:p.Thr250=
XM_011537701.1:c.750C>G	XP_011536003.1:p.Thr250=
XR_427781.2:n.804C>G
XR_944338.1:n.810C>G
XR_944339.1:n.810C>G
XM_005268524.5:c.744C>G	XP_005268581.1:p.Thr248=
XM_006714803.4:c.621C>G	XP_006714866.1:p.Thr207=
XM_011537698.3:c.750C>G	XP_011536000.1:p.Thr250=
XM_011537700.3:c.750C>G	XP_011536002.1:p.Thr250=
XM_011537701.3:c.750C>G	XP_011536003.1:p.Thr250=
XM_017010013.2:c.750C>G	XP_016865502.1:p.Thr250=
XR_002956197.1:n.746C>G
XR_427781.4:n.746C>G
XR_944338.3:n.825C>G
XR_944339.3:n.825C>G
NM_033449.3:c.750C>G MANE Select	NP_258260.1:p.Thr250=