Canonical Allele Identifier: CA2610736855
Gene: CNNM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103086429del , CM000672.2:g.103086429del GRCh38
NC_000010.10:g.104846186del , CM000672.1:g.104846186del GRCh37
NC_000010.9:g.104836176del NCBI36
NG_042272.1:g.111879del

Transcript Alleles

HGVS Amino-acid change
ENST00000369878.9:c.*9249del MANE Select ENSP00000358894.3:n.*9249del
ENST00000369878.8:c.*9249del ENSP00000358894.3:n.*9249del
XR_001747118.1:n.12130del
XR_001747121.1:n.12094del
NM_017649.5:c.*9249del MANE Select NP_060119.3:n.*9249del
NM_199076.3:c.*9249del NP_951058.1:n.*9249del