Canonical Allele Identifier: CA2722590141

Gene: CNNM2

Linked Data

• dbSNP Id: rs2134383785

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103086440_103086446del , CM000672.2:g.103086440_103086446del	GRCh38
NC_000010.10:g.104846197_104846203del , CM000672.1:g.104846197_104846203del	GRCh37
NC_000010.9:g.104836187_104836193del	NCBI36
NG_042272.1:g.111862_111868del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369878.9:c.*9260_*9266del MANE Select	ENSP00000358894.3:n.*9260_*9266del
ENST00000369878.8:c.*9260_*9266del	ENSP00000358894.3:n.*9260_*9266del
XR_001747118.1:n.12141_12147del
XR_001747121.1:n.12105_12111del
NM_017649.5:c.*9260_*9266del MANE Select	NP_060119.3:n.*9260_*9266del
NM_199076.3:c.*9260_*9266del	NP_951058.1:n.*9260_*9266del