Canonical Allele Identifier: CA1932995638

Gene: CNNM2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103086536_103086537delinsTG , CM000672.2:g.103086536_103086537delinsTG	GRCh38
NC_000010.10:g.104846293_104846294delinsTG , CM000672.1:g.104846293_104846294delinsTG	GRCh37
NC_000010.9:g.104836283_104836284delinsTG	NCBI36
NG_042272.1:g.111770_111771delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369878.9:c.*9356_*9357delinsTG MANE Select	ENSP00000358894.3:n.*9356_*9357delinsTG
ENST00000369878.8:c.*9356_*9357delinsTG	ENSP00000358894.3:n.*9356_*9357delinsTG
XR_001747118.1:n.12237_12238delinsTG
XR_001747121.1:n.12201_12202delinsTG
NM_017649.5:c.*9356_*9357delinsTG MANE Select	NP_060119.3:n.*9356_*9357delinsTG
NM_199076.3:c.*9356_*9357delinsTG	NP_951058.1:n.*9356_*9357delinsTG