Canonical Allele Identifier: CA2610736879

Gene: CNNM2

Linked Data

• gnomAD v4: 10-103086462-G-GCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103086462_103086463insCTGT , CM000672.2:g.103086462_103086463insCTGT	GRCh38
NC_000010.10:g.104846219_104846220insCTGT , CM000672.1:g.104846219_104846220insCTGT	GRCh37
NC_000010.9:g.104836209_104836210insCTGT	NCBI36
NG_042272.1:g.111844_111845insACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369878.9:c.*9282_*9283insCTGT MANE Select	ENSP00000358894.3:n.*9282_*9283insCTGT
ENST00000369878.8:c.*9282_*9283insCTGT	ENSP00000358894.3:n.*9282_*9283insCTGT
XR_001747118.1:n.12163_12164insCTGT
XR_001747121.1:n.12127_12128insCTGT
NM_017649.5:c.*9282_*9283insCTGT MANE Select	NP_060119.3:n.*9282_*9283insCTGT
NM_199076.3:c.*9282_*9283insCTGT	NP_951058.1:n.*9282_*9283insCTGT