Canonical Allele Identifier: CA804804503
Gene: FCHSD1 HGNC NCBI

Linked Data

dbSNP Id: rs1412964215

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141646880_141646881del , CM000667.2:g.141646880_141646881del GRCh38
NC_000005.9:g.141026447_141026448del , CM000667.1:g.141026447_141026448del GRCh37
NC_000005.8:g.141006631_141006632del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435817.7:c.925-158_925-157del MANE Select ENSP00000399259.2:n.925-158_925-157del
ENST00000435817.6:c.925-158_925-157del ENSP00000399259.2:n.925-158_925-157del
ENST00000522126.5:c.697-158_697-157del ENSP00000427796.1:n.697-158_697-157del
ENST00000522386.1:n.531-158_531-157del
ENST00000522763.5:n.229-158_229-157del
ENST00000522783.5:c.919-158_919-157del ENSP00000428677.1:n.919-158_919-157del
ENST00000523856.5:n.183-158_183-157del
NM_033449.2:c.925-158_925-157del NP_258260.1:n.925-158_925-157del
XM_005268524.3:c.919-158_919-157del XP_005268581.1:n.919-158_919-157del
XM_006714803.2:c.796-158_796-157del XP_006714866.1:n.796-158_796-157del
XM_011537698.1:c.925-158_925-157del XP_011536000.1:n.925-158_925-157del
XM_011537699.1:c.925-158_925-157del XP_011536001.1:n.925-158_925-157del
XM_011537700.1:c.925-158_925-157del XP_011536002.1:n.925-158_925-157del
XM_011537701.1:c.925-158_925-157del XP_011536003.1:n.925-158_925-157del
XR_427781.2:n.979-158_979-157del
XR_944338.1:n.985-158_985-157del
XR_944339.1:n.985-158_985-157del
XM_005268524.5:c.919-158_919-157del XP_005268581.1:n.919-158_919-157del
XM_006714803.4:c.796-158_796-157del XP_006714866.1:n.796-158_796-157del
XM_011537698.3:c.925-158_925-157del XP_011536000.1:n.925-158_925-157del
XM_011537700.3:c.925-158_925-157del XP_011536002.1:n.925-158_925-157del
XM_011537701.3:c.925-158_925-157del XP_011536003.1:n.925-158_925-157del
XM_017010013.2:c.925-158_925-157del XP_016865502.1:n.925-158_925-157del
XR_002956197.1:n.921-158_921-157del
XR_427781.4:n.921-158_921-157del
XR_944338.3:n.1000-158_1000-157del
XR_944339.3:n.1000-158_1000-157del
NM_033449.3:c.925-158_925-157del MANE Select NP_258260.1:n.925-158_925-157del