Canonical Allele Identifier: CA1759352141
Gene: CSMD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.4427524_4427528delinsAACAC , CM000670.2:g.4427524_4427528delinsAACAC GRCh38
NC_000008.10:g.4285046_4285050delinsAACAC , CM000670.1:g.4285046_4285050delinsAACAC GRCh37
NC_000008.9:g.4272454_4272458delinsAACAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000635120.2:c.303-7463_303-7459delinsGTGTT MANE Select ENSP00000489225.1:n.303-7463_303-7459delinsGTGTT
ENST00000400186.7:c.303-7463_303-7459delinsGTGTT ENSP00000383047.3:n.303-7463_303-7459delinsGTGTT
ENST00000520002.5:c.303-7463_303-7459delinsGTGTT ENSP00000430733.1:n.303-7463_303-7459delinsGTGTT
ENST00000602557.5:c.303-7463_303-7459delinsGTGTT ENSP00000473359.1:n.303-7463_303-7459delinsGTGTT
ENST00000602723.5:c.303-7463_303-7459delinsGTGTT ENSP00000473617.1:n.303-7463_303-7459delinsGTGTT
ENST00000635120.1:c.303-7463_303-7459delinsGTGTT ENSP00000489225.1:n.303-7463_303-7459delinsGTGTT
NM_033225.5:c.303-7463_303-7459delinsGTGTT NP_150094.5:n.303-7463_303-7459delinsGTGTT
XM_011534752.1:c.303-7463_303-7459delinsGTGTT XP_011533054.1:n.303-7463_303-7459delinsGTGTT
XM_011534752.2:c.303-7463_303-7459delinsGTGTT XP_011533054.1:n.303-7463_303-7459delinsGTGTT
XM_017013731.1:c.303-7463_303-7459delinsGTGTT XP_016869220.1:n.303-7463_303-7459delinsGTGTT
NM_033225.6:c.303-7463_303-7459delinsGTGTT MANE Select NP_150094.5:n.303-7463_303-7459delinsGTGTT