Canonical Allele Identifier: CA2610736874
Gene: CNNM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086462_103086463insATGT , CM000672.2:g.103086462_103086463insATGT GRCh38
NC_000010.10:g.104846219_104846220insATGT , CM000672.1:g.104846219_104846220insATGT GRCh37
NC_000010.9:g.104836209_104836210insATGT NCBI36
NG_042272.1:g.111844_111845insACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000369878.9:c.*9282_*9283insATGT MANE Select ENSP00000358894.3:n.*9282_*9283insATGT
ENST00000369878.8:c.*9282_*9283insATGT ENSP00000358894.3:n.*9282_*9283insATGT
XR_001747118.1:n.12163_12164insATGT
XR_001747121.1:n.12127_12128insATGT
NM_017649.5:c.*9282_*9283insATGT MANE Select NP_060119.3:n.*9282_*9283insATGT
NM_199076.3:c.*9282_*9283insATGT NP_951058.1:n.*9282_*9283insATGT