Canonical Allele Identifier: CA934282587
Gene: CDHR5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.616971_616975del , CM000673.2:g.616971_616975del GRCh38
NC_000011.9:g.616971_616975del , CM000673.1:g.616971_616975del GRCh37
NC_000011.8:g.606971_606975del NCBI36
NG_029106.1:g.4025_4029del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358353.8:c.*376_*380del ENSP00000351118.4:n.*376_*380del
ENST00000397542.7:c.*376_*380del MANE Select ENSP00000380676.2:n.*376_*380del
ENST00000358353.7:c.*376_*380del ENSP00000351118.3:n.*376_*380del
ENST00000397542.6:c.*376_*380del ENSP00000380676.2:n.*376_*380del
NM_001171968.1:c.*376_*380del NP_001165439.1:n.*376_*380del
NM_021924.4:c.*376_*380del NP_068743.2:n.*376_*380del
NM_031264.3:c.*376_*380del NP_112554.2:n.*376_*380del
XM_006718253.2:c.*376_*380del XP_006718316.1:n.*376_*380del
XM_011520188.1:c.*376_*380del XP_011518490.1:n.*376_*380del
XM_011520189.1:c.*376_*380del XP_011518491.1:n.*376_*380del
XM_011520190.1:c.*591_*595del XP_011518492.1:n.*591_*595del
XM_006718253.3:c.*376_*380del XP_006718316.1:n.*376_*380del
XM_011520188.2:c.*376_*380del XP_011518490.1:n.*376_*380del
XM_011520189.2:c.*376_*380del XP_011518491.1:n.*376_*380del
XM_011520190.2:c.*591_*595del XP_011518492.1:n.*591_*595del
NM_001171968.2:c.*376_*380del NP_001165439.2:n.*376_*380del
NM_021924.5:c.*376_*380del MANE Select NP_068743.3:n.*376_*380del
NM_031264.4:c.*376_*380del NP_112554.3:n.*376_*380del
NM_001171968.3:c.*376_*380del NP_001165439.2:n.*376_*380del
NM_031264.5:c.*376_*380del NP_112554.3:n.*376_*380del