Canonical Allele Identifier: CA1161506387

Gene: CSMD2

Linked Data

• dbSNP Id: rs1653868443

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.33517455T>G , CM000663.2:g.33517455T>G	GRCh38
NC_000001.10:g.33983055T>G , CM000663.1:g.33983055T>G	GRCh37
NC_000001.9:g.33755642T>G	NCBI36
NG_053181.1:g.653388A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373381.9:c.*54-885A>C MANE Select	ENSP00000362479.4:n.*54-885A>C
ENST00000373388.7:c.*54-885A>C	ENSP00000362486.3:n.*54-885A>C
ENST00000241312.8:c.*54-885A>C	ENSP00000241312.4:n.*54-885A>C
ENST00000373381.8:c.*54-885A>C	ENSP00000362479.4:n.*54-885A>C
ENST00000373388.6:c.*54-885A>C	ENSP00000362486.3:n.*54-885A>C
ENST00000619121.4:c.*54-885A>C	ENSP00000483463.1:n.*54-885A>C
NM_001281956.1:c.*54-885A>C	NP_001268885.1:n.*54-885A>C
NM_052896.4:c.*54-885A>C	NP_443128.2:n.*54-885A>C
XM_011540572.1:c.*179A>C	XP_011538874.1:n.*179A>C
XM_017000185.1:c.*2063A>C	XP_016855674.1:n.*2063A>C
XM_017000188.1:c.*2063A>C	XP_016855677.1:n.*2063A>C
XM_017000190.1:c.*2063A>C	XP_016855679.1:n.*2063A>C
XM_024452878.1:c.*2063A>C	XP_024308646.1:n.*2063A>C
XR_002959290.1:n.11049-885A>C
XR_002959291.1:n.10875-885A>C
XR_002959296.1:n.10784-885A>C
NM_001281956.2:c.*54-885A>C MANE Select	NP_001268885.1:n.*54-885A>C
NM_052896.5:c.*54-885A>C	NP_443128.2:n.*54-885A>C