Canonical Allele Identifier: CA563372879

Gene: FCHSD1

Linked Data

• dbSNP Id: rs1419211477
• gnomAD v2: 5-141026834-GACTC-G
• gnomAD v4: 5-141647267-GACTC-G
• MyVariant Identifiers: chr5:g.141026835_141026838del (hg19) ; chr5:g.141647268_141647271del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141647272_141647275del , CM000667.2:g.141647272_141647275del	GRCh38
NC_000005.9:g.141026839_141026842del , CM000667.1:g.141026839_141026842del	GRCh37
NC_000005.8:g.141007023_141007026del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435817.7:c.829-41_829-38del MANE Select	ENSP00000399259.2:n.829-41_829-38del
ENST00000435817.6:c.829-41_829-38del	ENSP00000399259.2:n.829-41_829-38del
ENST00000522126.5:c.601-41_601-38del	ENSP00000427796.1:n.601-41_601-38del
ENST00000522386.1:n.435-41_435-38del
ENST00000522763.5:n.133-41_133-38del
ENST00000522783.5:c.823-41_823-38del	ENSP00000428677.1:n.823-41_823-38del
ENST00000523856.5:n.87-41_87-38del
NM_033449.2:c.829-41_829-38del	NP_258260.1:n.829-41_829-38del
XM_005268524.3:c.823-41_823-38del	XP_005268581.1:n.823-41_823-38del
XM_006714803.2:c.700-41_700-38del	XP_006714866.1:n.700-41_700-38del
XM_011537698.1:c.829-41_829-38del	XP_011536000.1:n.829-41_829-38del
XM_011537699.1:c.829-41_829-38del	XP_011536001.1:n.829-41_829-38del
XM_011537700.1:c.829-41_829-38del	XP_011536002.1:n.829-41_829-38del
XM_011537701.1:c.829-41_829-38del	XP_011536003.1:n.829-41_829-38del
XR_427781.2:n.883-41_883-38del
XR_944338.1:n.889-41_889-38del
XR_944339.1:n.889-41_889-38del
XM_005268524.5:c.823-41_823-38del	XP_005268581.1:n.823-41_823-38del
XM_006714803.4:c.700-41_700-38del	XP_006714866.1:n.700-41_700-38del
XM_011537698.3:c.829-41_829-38del	XP_011536000.1:n.829-41_829-38del
XM_011537700.3:c.829-41_829-38del	XP_011536002.1:n.829-41_829-38del
XM_011537701.3:c.829-41_829-38del	XP_011536003.1:n.829-41_829-38del
XM_017010013.2:c.829-41_829-38del	XP_016865502.1:n.829-41_829-38del
XR_002956197.1:n.825-41_825-38del
XR_427781.4:n.825-41_825-38del
XR_944338.3:n.904-41_904-38del
XR_944339.3:n.904-41_904-38del
NM_033449.3:c.829-41_829-38del MANE Select	NP_258260.1:n.829-41_829-38del