Canonical Allele Identifier: CA1759352700
Gene: CSMD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.4428147_4428148delinsCA , CM000670.2:g.4428147_4428148delinsCA GRCh38
NC_000008.10:g.4285669_4285670delinsCA , CM000670.1:g.4285669_4285670delinsCA GRCh37
NC_000008.9:g.4273077_4273078delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000635120.2:c.303-8083_303-8082delinsTG MANE Select ENSP00000489225.1:n.303-8083_303-8082delinsTG
ENST00000400186.7:c.303-8083_303-8082delinsTG ENSP00000383047.3:n.303-8083_303-8082delinsTG
ENST00000520002.5:c.303-8083_303-8082delinsTG ENSP00000430733.1:n.303-8083_303-8082delinsTG
ENST00000602557.5:c.303-8083_303-8082delinsTG ENSP00000473359.1:n.303-8083_303-8082delinsTG
ENST00000602723.5:c.303-8083_303-8082delinsTG ENSP00000473617.1:n.303-8083_303-8082delinsTG
ENST00000635120.1:c.303-8083_303-8082delinsTG ENSP00000489225.1:n.303-8083_303-8082delinsTG
NM_033225.5:c.303-8083_303-8082delinsTG NP_150094.5:n.303-8083_303-8082delinsTG
XM_011534752.1:c.303-8083_303-8082delinsTG XP_011533054.1:n.303-8083_303-8082delinsTG
XM_011534752.2:c.303-8083_303-8082delinsTG XP_011533054.1:n.303-8083_303-8082delinsTG
XM_017013731.1:c.303-8083_303-8082delinsTG XP_016869220.1:n.303-8083_303-8082delinsTG
NM_033225.6:c.303-8083_303-8082delinsTG MANE Select NP_150094.5:n.303-8083_303-8082delinsTG