Canonical Allele Identifier: CA170978026
Gene: CSMD1 HGNC NCBI

Linked Data

dbSNP Id: rs912191915

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.4285529A>G , CM000670.2:g.4285529A>G GRCh38
NC_000008.10:g.4143051A>G , CM000670.1:g.4143051A>G GRCh37
NC_000008.9:g.4130459A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000635120.2:c.415+134424T>C MANE Select ENSP00000489225.1:n.415+134424T>C
ENST00000400186.7:c.415+134424T>C ENSP00000383047.3:n.415+134424T>C
ENST00000520002.5:c.415+134424T>C ENSP00000430733.1:n.415+134424T>C
ENST00000602557.5:c.415+134424T>C ENSP00000473359.1:n.415+134424T>C
ENST00000602723.5:c.415+134424T>C ENSP00000473617.1:n.415+134424T>C
ENST00000635120.1:c.415+134424T>C ENSP00000489225.1:n.415+134424T>C
NM_033225.5:c.415+134424T>C NP_150094.5:n.415+134424T>C
XM_011534752.1:c.415+134424T>C XP_011533054.1:n.415+134424T>C
XM_011534752.2:c.415+134424T>C XP_011533054.1:n.415+134424T>C
XM_017013731.1:c.415+134424T>C XP_016869220.1:n.415+134424T>C
NM_033225.6:c.415+134424T>C MANE Select NP_150094.5:n.415+134424T>C