Canonical Allele Identifier: CA2610736875

Gene: CNNM2

Linked Data

• gnomAD v4: 10-103086462-G-GTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103086464_103086465insTTTT , CM000672.2:g.103086464_103086465insTTTT	GRCh38
NC_000010.10:g.104846221_104846222insTTTT , CM000672.1:g.104846221_104846222insTTTT	GRCh37
NC_000010.9:g.104836211_104836212insTTTT	NCBI36
NG_042272.1:g.111844_111845insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369878.9:c.*9284_*9285insTTTT MANE Select	ENSP00000358894.3:n.*9284_*9285insTTTT
ENST00000369878.8:c.*9284_*9285insTTTT	ENSP00000358894.3:n.*9284_*9285insTTTT
XR_001747118.1:n.12165_12166insTTTT
XR_001747121.1:n.12129_12130insTTTT
NM_017649.5:c.*9284_*9285insTTTT MANE Select	NP_060119.3:n.*9284_*9285insTTTT
NM_199076.3:c.*9284_*9285insTTTT	NP_951058.1:n.*9284_*9285insTTTT