Canonical Allele Identifier: CA1109930885

Gene: CSMD1

Linked Data

• dbSNP Id: rs1797007889
• gnomAD v3: 8-4285434-A-T
• gnomAD v4: 8-4285434-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.4285434A>T , CM000670.2:g.4285434A>T	GRCh38
NC_000008.10:g.4142956A>T , CM000670.1:g.4142956A>T	GRCh37
NC_000008.9:g.4130364A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000635120.2:c.415+134519T>A MANE Select	ENSP00000489225.1:n.415+134519T>A
ENST00000400186.7:c.415+134519T>A	ENSP00000383047.3:n.415+134519T>A
ENST00000520002.5:c.415+134519T>A	ENSP00000430733.1:n.415+134519T>A
ENST00000602557.5:c.415+134519T>A	ENSP00000473359.1:n.415+134519T>A
ENST00000602723.5:c.415+134519T>A	ENSP00000473617.1:n.415+134519T>A
ENST00000635120.1:c.415+134519T>A	ENSP00000489225.1:n.415+134519T>A
NM_033225.5:c.415+134519T>A	NP_150094.5:n.415+134519T>A
XM_011534752.1:c.415+134519T>A	XP_011533054.1:n.415+134519T>A
XM_011534752.2:c.415+134519T>A	XP_011533054.1:n.415+134519T>A
XM_017013731.1:c.415+134519T>A	XP_016869220.1:n.415+134519T>A
NM_033225.6:c.415+134519T>A MANE Select	NP_150094.5:n.415+134519T>A