Canonical Allele Identifier: CA1932995593
Gene: CNNM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086423_103086424delinsTG , CM000672.2:g.103086423_103086424delinsTG GRCh38
NC_000010.10:g.104846180_104846181delinsTG , CM000672.1:g.104846180_104846181delinsTG GRCh37
NC_000010.9:g.104836170_104836171delinsTG NCBI36
NG_042272.1:g.111883_111884delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9243_*9244delinsTG MANE Select ENSP00000358894.3:n.*9243_*9244delinsTG
ENST00000369878.8:c.*9243_*9244delinsTG ENSP00000358894.3:n.*9243_*9244delinsTG
XR_001747118.1:n.12124_12125delinsTG
XR_001747121.1:n.12088_12089delinsTG
NM_017649.5:c.*9243_*9244delinsTG MANE Select NP_060119.3:n.*9243_*9244delinsTG
NM_199076.3:c.*9243_*9244delinsTG NP_951058.1:n.*9243_*9244delinsTG