Canonical Allele Identifier: CA1811352877

Gene: CSMD3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.112255869G= , CM000670.2:g.112255869G=	GRCh38
NC_000008.10:g.113268098G= , CM000670.1:g.113268098G=	GRCh37
NC_000008.9:g.113337274G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_198123.2:c.9863-442C= MANE Select	NP_937756.1:n.9863-442C=
ENST00000297405.10:c.9863-442C= MANE Select	ENSP00000297405.5:n.9863-442C=
NM_001363185.1:c.9263-442C=	NP_001350114.1:n.9263-442C=
NM_052900.2:c.9356-442C=	NP_443132.3:n.9356-442C=
NM_052900.3:c.9356-442C=	NP_443132.3:n.9356-442C=
NM_198123.1:c.9863-442C=	NP_937756.1:n.9863-442C=
NM_198124.1:c.9743-442C=	NP_937757.1:n.9743-442C=
NM_198124.2:c.9743-442C=	NP_937757.1:n.9743-442C=
ENST00000297405.9:c.9863-442C=	ENSP00000297405.5:n.9863-442C=
ENST00000339701.7:c.7673-442C=	ENSP00000341558.3:n.7673-442C=
ENST00000343508.7:c.9743-442C=	ENSP00000345799.3:n.9743-442C=
ENST00000455883.2:c.9356-442C=	ENSP00000412263.2:n.9356-442C=
ENST00000534172.1:n.60C=
XM_011516808.1:c.9665-442C=	XP_011515110.1:n.9665-442C=
XM_011516809.1:c.9425-442C=	XP_011515111.1:n.9425-442C=
XM_011516810.1:c.9353-442C=	XP_011515112.1:n.9353-442C=
XM_011516811.1:c.7967-442C=	XP_011515113.1:n.7967-442C=
XM_011516813.1:c.7139-442C=	XP_011515115.1:n.7139-442C=
XM_011516815.1:c.5261-442C=	XP_011515117.1:n.5261-442C=
XM_011516815.2:c.5261-442C=	XP_011515117.1:n.5261-442C=
XM_011516816.1:c.9551-442C=	XP_011515118.1:n.9551-442C=
XM_011516816.2:c.9551-442C=	XP_011515118.1:n.9551-442C=
XM_017013008.1:c.9785-442C=	XP_016868497.1:n.9785-442C=
XM_017013009.2:c.9653-442C=	XP_016868498.1:n.9653-442C=
XM_017013010.1:c.9473-442C=	XP_016868499.1:n.9473-442C=
XM_017013012.1:c.9131-442C=	XP_016868501.1:n.9131-442C=