Canonical Allele Identifier: CA171047600
Gene: CSMD1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1154053

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.4427868G>C , CM000670.2:g.4427868G>C GRCh38
NC_000008.10:g.4285390G>C , CM000670.1:g.4285390G>C GRCh37
NC_000008.9:g.4272798G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_033225.5:c.303-7803C>G VV NP_150094.5:p.=
XM_011534752.1:c.303-7803C>G XP_011533054.1:p.=
XM_011534752.2:c.303-7803C>G
XM_017013731.1:c.303-7803C>G XP_016869220.1:p.=
ENST00000400186.7:c.303-7803C>G ENSP00000383047.3:p.=
ENST00000520002.5:c.303-7803C>G ENSP00000430733.1:p.=
ENST00000602557.5:c.303-7803C>G ENSP00000473359.1:p.=
ENST00000602723.5:c.303-7803C>G ENSP00000473617.1:p.=
ENST00000635120.1:c.303-7803C>G ENSP00000489225.1:p.=