Canonical Allele Identifier: CA2578433885

Gene: FCHSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647381del , CM000667.2:g.141647381del	GRCh38
NC_000005.9:g.141026948del , CM000667.1:g.141026948del	GRCh37
NC_000005.8:g.141007132del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.828+17del MANE Select	ENSP00000399259.2:n.828+17del
ENST00000435817.6:c.828+17del	ENSP00000399259.2:n.828+17del
ENST00000522126.5:c.600+17del	ENSP00000427796.1:n.600+17del
ENST00000522386.1:n.434+17del
ENST00000522763.5:n.132+17del
ENST00000522783.5:c.822+17del	ENSP00000428677.1:n.822+17del
ENST00000523856.5:n.86+17del
NM_033449.2:c.828+17del	NP_258260.1:n.828+17del
XM_005268524.3:c.822+17del	XP_005268581.1:n.822+17del
XM_006714803.2:c.699+17del	XP_006714866.1:n.699+17del
XM_011537698.1:c.828+17del	XP_011536000.1:n.828+17del
XM_011537699.1:c.828+17del	XP_011536001.1:n.828+17del
XM_011537700.1:c.828+17del	XP_011536002.1:n.828+17del
XM_011537701.1:c.828+17del	XP_011536003.1:n.828+17del
XR_427781.2:n.882+17del
XR_944338.1:n.888+17del
XR_944339.1:n.888+17del
XM_005268524.5:c.822+17del	XP_005268581.1:n.822+17del
XM_006714803.4:c.699+17del	XP_006714866.1:n.699+17del
XM_011537698.3:c.828+17del	XP_011536000.1:n.828+17del
XM_011537700.3:c.828+17del	XP_011536002.1:n.828+17del
XM_011537701.3:c.828+17del	XP_011536003.1:n.828+17del
XM_017010013.2:c.828+17del	XP_016865502.1:n.828+17del
XR_002956197.1:n.824+17del
XR_427781.4:n.824+17del
XR_944338.3:n.903+17del
XR_944339.3:n.903+17del
NM_033449.3:c.828+17del MANE Select	NP_258260.1:n.828+17del