Canonical Allele Identifier: CA1759352063

Gene: CSMD1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.4427468_4427471delinsTCAG , CM000670.2:g.4427468_4427471delinsTCAG	GRCh38
NC_000008.10:g.4284990_4284993delinsTCAG , CM000670.1:g.4284990_4284993delinsTCAG	GRCh37
NC_000008.9:g.4272398_4272401delinsTCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635120.2:c.303-7406_303-7403delinsCTGA MANE Select	ENSP00000489225.1:n.303-7406_303-7403delinsCTGA
ENST00000400186.7:c.303-7406_303-7403delinsCTGA	ENSP00000383047.3:n.303-7406_303-7403delinsCTGA
ENST00000520002.5:c.303-7406_303-7403delinsCTGA	ENSP00000430733.1:n.303-7406_303-7403delinsCTGA
ENST00000602557.5:c.303-7406_303-7403delinsCTGA	ENSP00000473359.1:n.303-7406_303-7403delinsCTGA
ENST00000602723.5:c.303-7406_303-7403delinsCTGA	ENSP00000473617.1:n.303-7406_303-7403delinsCTGA
ENST00000635120.1:c.303-7406_303-7403delinsCTGA	ENSP00000489225.1:n.303-7406_303-7403delinsCTGA
NM_033225.5:c.303-7406_303-7403delinsCTGA	NP_150094.5:n.303-7406_303-7403delinsCTGA
XM_011534752.1:c.303-7406_303-7403delinsCTGA	XP_011533054.1:n.303-7406_303-7403delinsCTGA
XM_011534752.2:c.303-7406_303-7403delinsCTGA	XP_011533054.1:n.303-7406_303-7403delinsCTGA
XM_017013731.1:c.303-7406_303-7403delinsCTGA	XP_016869220.1:n.303-7406_303-7403delinsCTGA
NM_033225.6:c.303-7406_303-7403delinsCTGA MANE Select	NP_150094.5:n.303-7406_303-7403delinsCTGA