Canonical Allele Identifier: CA128463374

Gene: FCHSD1

Linked Data

• dbSNP Id: rs1013026558
• gnomAD v2: 5-141026967-G-A
• gnomAD v3: 5-141647400-G-A
• gnomAD v4: 5-141647400-G-A
• MyVariant Identifiers: chr5:g.141026967G>A (hg19) ; chr5:g.141647400G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647400G>A , CM000667.2:g.141647400G>A	GRCh38
NC_000005.9:g.141026967G>A , CM000667.1:g.141026967G>A	GRCh37
NC_000005.8:g.141007151G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.826C>T MANE Select	ENSP00000399259.2:p.Gln276Ter
ENST00000435817.6:c.826C>T	ENSP00000399259.2:p.Gln276Ter
ENST00000522126.5:c.598C>T	ENSP00000427796.1:p.Gln200Ter
ENST00000522386.1:n.432C>T
ENST00000522763.5:n.130C>T
ENST00000522783.5:c.820C>T	ENSP00000428677.1:p.Gln274Ter
ENST00000523856.5:n.84C>T
NM_033449.2:c.826C>T	NP_258260.1:p.Gln276Ter
XM_005268524.3:c.820C>T	XP_005268581.1:p.Gln274Ter
XM_006714803.2:c.697C>T	XP_006714866.1:p.Gln233Ter
XM_011537698.1:c.826C>T	XP_011536000.1:p.Gln276Ter
XM_011537699.1:c.826C>T	XP_011536001.1:p.Gln276Ter
XM_011537700.1:c.826C>T	XP_011536002.1:p.Gln276Ter
XM_011537701.1:c.826C>T	XP_011536003.1:p.Gln276Ter
XR_427781.2:n.880C>T
XR_944338.1:n.886C>T
XR_944339.1:n.886C>T
XM_005268524.5:c.820C>T	XP_005268581.1:p.Gln274Ter
XM_006714803.4:c.697C>T	XP_006714866.1:p.Gln233Ter
XM_011537698.3:c.826C>T	XP_011536000.1:p.Gln276Ter
XM_011537700.3:c.826C>T	XP_011536002.1:p.Gln276Ter
XM_011537701.3:c.826C>T	XP_011536003.1:p.Gln276Ter
XM_017010013.2:c.826C>T	XP_016865502.1:p.Gln276Ter
XR_002956197.1:n.822C>T
XR_427781.4:n.822C>T
XR_944338.3:n.901C>T
XR_944339.3:n.901C>T
NM_033449.3:c.826C>T MANE Select	NP_258260.1:p.Gln276Ter