Canonical Allele Identifier: CA1759222281

Gene: CSMD1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.4285453G= , CM000670.2:g.4285453G=	GRCh38
NC_000008.10:g.4142975G= , CM000670.1:g.4142975G=	GRCh37
NC_000008.9:g.4130383G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000635120.2:c.415+134500C= MANE Select	ENSP00000489225.1:n.415+134500C=
ENST00000400186.7:c.415+134500C=	ENSP00000383047.3:n.415+134500C=
ENST00000520002.5:c.415+134500C=	ENSP00000430733.1:n.415+134500C=
ENST00000602557.5:c.415+134500C=	ENSP00000473359.1:n.415+134500C=
ENST00000602723.5:c.415+134500C=	ENSP00000473617.1:n.415+134500C=
ENST00000635120.1:c.415+134500C=	ENSP00000489225.1:n.415+134500C=
NM_033225.5:c.415+134500C=	NP_150094.5:n.415+134500C=
XM_011534752.1:c.415+134500C=	XP_011533054.1:n.415+134500C=
XM_011534752.2:c.415+134500C=	XP_011533054.1:n.415+134500C=
XM_017013731.1:c.415+134500C=	XP_016869220.1:n.415+134500C=
NM_033225.6:c.415+134500C= MANE Select	NP_150094.5:n.415+134500C=