Canonical Allele Identifier: CA563372882
Gene: FCHSD1 HGNC NCBI

Linked Data

dbSNP Id: rs1163276881

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141647274T>C , CM000667.2:g.141647274T>C GRCh38
NC_000005.9:g.141026841T>C , CM000667.1:g.141026841T>C GRCh37
NC_000005.8:g.141007025T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435817.7:c.829-44A>G MANE Select ENSP00000399259.2:n.829-44A>G
ENST00000435817.6:c.829-44A>G ENSP00000399259.2:n.829-44A>G
ENST00000522126.5:c.601-44A>G ENSP00000427796.1:n.601-44A>G
ENST00000522386.1:n.435-44A>G
ENST00000522763.5:n.133-44A>G
ENST00000522783.5:c.823-44A>G ENSP00000428677.1:n.823-44A>G
ENST00000523856.5:n.87-44A>G
NM_033449.2:c.829-44A>G NP_258260.1:n.829-44A>G
XM_005268524.3:c.823-44A>G XP_005268581.1:n.823-44A>G
XM_006714803.2:c.700-44A>G XP_006714866.1:n.700-44A>G
XM_011537698.1:c.829-44A>G XP_011536000.1:n.829-44A>G
XM_011537699.1:c.829-44A>G XP_011536001.1:n.829-44A>G
XM_011537700.1:c.829-44A>G XP_011536002.1:n.829-44A>G
XM_011537701.1:c.829-44A>G XP_011536003.1:n.829-44A>G
XR_427781.2:n.883-44A>G
XR_944338.1:n.889-44A>G
XR_944339.1:n.889-44A>G
XM_005268524.5:c.823-44A>G XP_005268581.1:n.823-44A>G
XM_006714803.4:c.700-44A>G XP_006714866.1:n.700-44A>G
XM_011537698.3:c.829-44A>G XP_011536000.1:n.829-44A>G
XM_011537700.3:c.829-44A>G XP_011536002.1:n.829-44A>G
XM_011537701.3:c.829-44A>G XP_011536003.1:n.829-44A>G
XM_017010013.2:c.829-44A>G XP_016865502.1:n.829-44A>G
XR_002956197.1:n.825-44A>G
XR_427781.4:n.825-44A>G
XR_944338.3:n.904-44A>G
XR_944339.3:n.904-44A>G
NM_033449.3:c.829-44A>G MANE Select NP_258260.1:n.829-44A>G