Canonical Allele Identifier: CA1758603518

Gene: CSMD1

Linked Data

• dbSNP Id: rs7829759

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.3289837A>T , CM000670.2:g.3289837A>T	GRCh38
NC_000008.10:g.3147359A>T , CM000670.1:g.3147359A>T	GRCh37
NC_000008.9:g.3134766A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000635120.2:c.3951-5491T>A MANE Select	ENSP00000489225.1:n.3951-5491T>A
ENST00000335551.11:c.2392-5491T>A
ENST00000400186.7:c.3954-5491T>A	ENSP00000383047.3:n.3954-5491T>A
ENST00000520002.5:c.3954-5491T>A	ENSP00000430733.1:n.3954-5491T>A
ENST00000523488.5:n.1484-5491T>A
ENST00000537824.2:c.3537-5491T>A	ENSP00000441462.2:n.3537-5491T>A
ENST00000602557.5:c.3954-5491T>A	ENSP00000473359.1:n.3954-5491T>A
ENST00000602723.5:c.3954-5491T>A	ENSP00000473617.1:n.3954-5491T>A
ENST00000635120.1:c.3951-5491T>A	ENSP00000489225.1:n.3951-5491T>A
NM_033225.5:c.3951-5491T>A	NP_150094.5:n.3951-5491T>A
XM_011534752.1:c.3951-5491T>A	XP_011533054.1:n.3951-5491T>A
XM_011534753.1:c.1044-5491T>A	XP_011533055.1:n.1044-5491T>A
XM_011534752.2:c.3951-5491T>A	XP_011533054.1:n.3951-5491T>A
XM_011534753.3:c.1044-5491T>A	XP_011533055.1:n.1044-5491T>A
XM_017013731.1:c.3951-5491T>A	XP_016869220.1:n.3951-5491T>A
NM_033225.6:c.3951-5491T>A MANE Select	NP_150094.5:n.3951-5491T>A