Canonical Allele Identifier: CA212317696
Gene: CNNM2 HGNC NCBI

Linked Data

dbSNP Id: rs200257798
MyVariant Identifiers: chr10:g.104846218_104846219insGTT (hg19) chr10:g.103086461_103086462insGTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086464_103086466dup , CM000672.2:g.103086464_103086466dup GRCh38
NC_000010.10:g.104846221_104846223dup , CM000672.1:g.104846221_104846223dup GRCh37
NC_000010.9:g.104836211_104836213dup NCBI36
NG_042272.1:g.111843_111845dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369878.9:c.*9284_*9286dup MANE Select ENSP00000358894.3:n.*9284_*9286dup
ENST00000369878.8:c.*9284_*9286dup ENSP00000358894.3:n.*9284_*9286dup
XR_001747118.1:n.12165_12167dup
XR_001747121.1:n.12129_12131dup
NM_017649.5:c.*9284_*9286dup MANE Select NP_060119.3:n.*9284_*9286dup
NM_199076.3:c.*9284_*9286dup NP_951058.1:n.*9284_*9286dup
Search 100 bp 5'
Search 100 bp 3'