Canonical Allele Identifier: CA170742329

Gene: CSMD1

Linked Data

• dbSNP Id: rs1001965782
• MyVariant Identifiers: chr8:g.3091510G>A (hg19) ; chr8:g.3233988G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.3233988G>A , CM000670.2:g.3233988G>A	GRCh38
NC_000008.10:g.3091510G>A , CM000670.1:g.3091510G>A	GRCh37
NC_000008.9:g.3078917G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635120.2:c.4154-3757C>T MANE Select	ENSP00000489225.1:n.4154-3757C>T
ENST00000335551.11:c.2595-3757C>T
ENST00000400186.7:c.4157-3757C>T	ENSP00000383047.3:n.4157-3757C>T
ENST00000520002.5:c.4157-3757C>T	ENSP00000430733.1:n.4157-3757C>T
ENST00000523387.5:n.387-3757C>T
ENST00000523488.5:n.1687-3757C>T
ENST00000537824.2:c.3740-3757C>T	ENSP00000441462.2:n.3740-3757C>T
ENST00000602557.5:c.4157-3757C>T	ENSP00000473359.1:n.4157-3757C>T
ENST00000602723.5:c.4157-3757C>T	ENSP00000473617.1:n.4157-3757C>T
ENST00000635120.1:c.4154-3757C>T	ENSP00000489225.1:n.4154-3757C>T
NM_033225.5:c.4154-3757C>T	NP_150094.5:n.4154-3757C>T
XM_011534752.1:c.4154-3757C>T	XP_011533054.1:n.4154-3757C>T
XM_011534753.1:c.1247-3757C>T	XP_011533055.1:n.1247-3757C>T
XM_011534754.1:c.176-3757C>T	XP_011533056.1:n.176-3757C>T
XM_011534752.2:c.4154-3757C>T	XP_011533054.1:n.4154-3757C>T
XM_011534753.3:c.1247-3757C>T	XP_011533055.1:n.1247-3757C>T
XM_017013731.1:c.4154-3757C>T	XP_016869220.1:n.4154-3757C>T
NM_033225.6:c.4154-3757C>T MANE Select	NP_150094.5:n.4154-3757C>T