Canonical Allele Identifier: CA1758603834

Gene: CSMD1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.3289967A= , CM000670.2:g.3289967A=	GRCh38
NC_000008.10:g.3147489A= , CM000670.1:g.3147489A=	GRCh37
NC_000008.9:g.3134896A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635120.2:c.3951-5621T= MANE Select	ENSP00000489225.1:n.3951-5621T=
ENST00000335551.11:c.2392-5621T=
ENST00000400186.7:c.3954-5621T=	ENSP00000383047.3:n.3954-5621T=
ENST00000520002.5:c.3954-5621T=	ENSP00000430733.1:n.3954-5621T=
ENST00000523488.5:n.1484-5621T=
ENST00000537824.2:c.3537-5621T=	ENSP00000441462.2:n.3537-5621T=
ENST00000602557.5:c.3954-5621T=	ENSP00000473359.1:n.3954-5621T=
ENST00000602723.5:c.3954-5621T=	ENSP00000473617.1:n.3954-5621T=
ENST00000635120.1:c.3951-5621T=	ENSP00000489225.1:n.3951-5621T=
NM_033225.5:c.3951-5621T=	NP_150094.5:n.3951-5621T=
XM_011534752.1:c.3951-5621T=	XP_011533054.1:n.3951-5621T=
XM_011534753.1:c.1044-5621T=	XP_011533055.1:n.1044-5621T=
XM_011534752.2:c.3951-5621T=	XP_011533054.1:n.3951-5621T=
XM_011534753.3:c.1044-5621T=	XP_011533055.1:n.1044-5621T=
XM_017013731.1:c.3951-5621T=	XP_016869220.1:n.3951-5621T=
NM_033225.6:c.3951-5621T= MANE Select	NP_150094.5:n.3951-5621T=