Canonical Allele Identifier: CA1109983454

Gene: CSMD1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.4625619A>C , CM000670.2:g.4625619A>C	GRCh38
NC_000008.10:g.4483141A>C , CM000670.1:g.4483141A>C	GRCh37
NC_000008.9:g.4470549A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635120.2:c.302+11723T>G MANE Select	ENSP00000489225.1:n.302+11723T>G
ENST00000400186.7:c.302+11723T>G	ENSP00000383047.3:n.302+11723T>G
ENST00000520002.5:c.302+11723T>G	ENSP00000430733.1:n.302+11723T>G
ENST00000602557.5:c.302+11723T>G	ENSP00000473359.1:n.302+11723T>G
ENST00000602723.5:c.302+11723T>G	ENSP00000473617.1:n.302+11723T>G
ENST00000635120.1:c.302+11723T>G	ENSP00000489225.1:n.302+11723T>G
NM_033225.5:c.302+11723T>G	NP_150094.5:n.302+11723T>G
XM_011534752.1:c.302+11723T>G	XP_011533054.1:n.302+11723T>G
XM_011534752.2:c.302+11723T>G	XP_011533054.1:n.302+11723T>G
XM_017013731.1:c.302+11723T>G	XP_016869220.1:n.302+11723T>G
NM_033225.6:c.302+11723T>G MANE Select	NP_150094.5:n.302+11723T>G