Canonical Allele Identifier: CA2611720841
Gene: CDHR5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.616968_616973del , CM000673.2:g.616968_616973del GRCh38
NC_000011.9:g.616968_616973del , CM000673.1:g.616968_616973del GRCh37
NC_000011.8:g.606968_606973del NCBI36
NG_029106.1:g.4027_4032del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358353.8:c.*378_*383del ENSP00000351118.4:n.*378_*383del
ENST00000397542.7:c.*378_*383del MANE Select ENSP00000380676.2:n.*378_*383del
ENST00000358353.7:c.*378_*383del ENSP00000351118.3:n.*378_*383del
ENST00000397542.6:c.*378_*383del ENSP00000380676.2:n.*378_*383del
NM_001171968.1:c.*378_*383del NP_001165439.1:n.*378_*383del
NM_021924.4:c.*378_*383del NP_068743.2:n.*378_*383del
NM_031264.3:c.*378_*383del NP_112554.2:n.*378_*383del
XM_006718253.2:c.*378_*383del XP_006718316.1:n.*378_*383del
XM_011520188.1:c.*378_*383del XP_011518490.1:n.*378_*383del
XM_011520189.1:c.*378_*383del XP_011518491.1:n.*378_*383del
XM_011520190.1:c.*593_*598del XP_011518492.1:n.*593_*598del
XM_006718253.3:c.*378_*383del XP_006718316.1:n.*378_*383del
XM_011520188.2:c.*378_*383del XP_011518490.1:n.*378_*383del
XM_011520189.2:c.*378_*383del XP_011518491.1:n.*378_*383del
XM_011520190.2:c.*593_*598del XP_011518492.1:n.*593_*598del
NM_001171968.2:c.*378_*383del NP_001165439.2:n.*378_*383del
NM_021924.5:c.*378_*383del MANE Select NP_068743.3:n.*378_*383del
NM_031264.4:c.*378_*383del NP_112554.3:n.*378_*383del
NM_001171968.3:c.*378_*383del NP_001165439.2:n.*378_*383del
NM_031264.5:c.*378_*383del NP_112554.3:n.*378_*383del