Canonical Allele Identifier: CA446897304

Gene: FCHSD1

Linked Data

• MyVariant Identifiers: chr5:g.141027001C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647434C>G , CM000667.2:g.141647434C>G	GRCh38
NC_000005.9:g.141027001C>G , CM000667.1:g.141027001C>G	GRCh37
NC_000005.8:g.141007185C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.792G>C MANE Select	ENSP00000399259.2:p.Leu264=
ENST00000435817.6:c.792G>C	ENSP00000399259.2:p.Leu264=
ENST00000522126.5:c.564G>C	ENSP00000427796.1:p.Leu188=
ENST00000522386.1:n.398G>C
ENST00000522763.5:n.96G>C
ENST00000522783.5:c.786G>C	ENSP00000428677.1:p.Leu262=
ENST00000523856.5:n.50G>C
NM_033449.2:c.792G>C	NP_258260.1:p.Leu264=
XM_005268524.3:c.786G>C	XP_005268581.1:p.Leu262=
XM_006714803.2:c.663G>C	XP_006714866.1:p.Leu221=
XM_011537698.1:c.792G>C	XP_011536000.1:p.Leu264=
XM_011537699.1:c.792G>C	XP_011536001.1:p.Leu264=
XM_011537700.1:c.792G>C	XP_011536002.1:p.Leu264=
XM_011537701.1:c.792G>C	XP_011536003.1:p.Leu264=
XR_427781.2:n.846G>C
XR_944338.1:n.852G>C
XR_944339.1:n.852G>C
XM_005268524.5:c.786G>C	XP_005268581.1:p.Leu262=
XM_006714803.4:c.663G>C	XP_006714866.1:p.Leu221=
XM_011537698.3:c.792G>C	XP_011536000.1:p.Leu264=
XM_011537700.3:c.792G>C	XP_011536002.1:p.Leu264=
XM_011537701.3:c.792G>C	XP_011536003.1:p.Leu264=
XM_017010013.2:c.792G>C	XP_016865502.1:p.Leu264=
XR_002956197.1:n.788G>C
XR_427781.4:n.788G>C
XR_944338.3:n.867G>C
XR_944339.3:n.867G>C
NM_033449.3:c.792G>C MANE Select	NP_258260.1:p.Leu264=