Canonical Allele Identifier: CA1947210609
Gene: CDHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.616709G= , CM000673.2:g.616709G= GRCh38
NC_000011.9:g.616709G= , CM000673.1:g.616709G= GRCh37
NC_000011.8:g.606709G= NCBI36
NG_029106.1:g.4291C=

Transcript Alleles

HGVS Amino-acid change
ENST00000358353.8:c.*642C= ENSP00000351118.4:n.*642C=
ENST00000397542.7:c.*642C= MANE Select ENSP00000380676.2:n.*642C=
ENST00000358353.7:c.*642C= ENSP00000351118.3:n.*642C=
ENST00000397542.6:c.*642C= ENSP00000380676.2:n.*642C=
NM_001171968.1:c.*642C= NP_001165439.1:n.*642C=
NM_021924.4:c.*642C= NP_068743.2:n.*642C=
NM_031264.3:c.*642C= NP_112554.2:n.*642C=
XM_006718253.2:c.*642C= XP_006718316.1:n.*642C=
XM_011520188.1:c.*642C= XP_011518490.1:n.*642C=
XM_011520189.1:c.*642C= XP_011518491.1:n.*642C=
XM_011520190.1:c.*857C= XP_011518492.1:n.*857C=
XM_006718253.3:c.*642C= XP_006718316.1:n.*642C=
XM_011520188.2:c.*642C= XP_011518490.1:n.*642C=
XM_011520189.2:c.*642C= XP_011518491.1:n.*642C=
XM_011520190.2:c.*857C= XP_011518492.1:n.*857C=
NM_001171968.2:c.*642C= NP_001165439.2:n.*642C=
NM_021924.5:c.*642C= MANE Select NP_068743.3:n.*642C=
NM_031264.4:c.*642C= NP_112554.3:n.*642C=
NM_001171968.3:c.*642C= NP_001165439.2:n.*642C=
NM_031264.5:c.*642C= NP_112554.3:n.*642C=