Canonical Allele Identifier: CA1947210769
Gene: CDHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.616798A= , CM000673.2:g.616798A= GRCh38
NC_000011.9:g.616798A= , CM000673.1:g.616798A= GRCh37
NC_000011.8:g.606798A= NCBI36
NG_029106.1:g.4202T=

Transcript Alleles

HGVS Amino-acid change
ENST00000358353.8:c.*553T= ENSP00000351118.4:n.*553T=
ENST00000397542.7:c.*553T= MANE Select ENSP00000380676.2:n.*553T=
ENST00000358353.7:c.*553T= ENSP00000351118.3:n.*553T=
ENST00000397542.6:c.*553T= ENSP00000380676.2:n.*553T=
NM_001171968.1:c.*553T= NP_001165439.1:n.*553T=
NM_021924.4:c.*553T= NP_068743.2:n.*553T=
NM_031264.3:c.*553T= NP_112554.2:n.*553T=
XM_006718253.2:c.*553T= XP_006718316.1:n.*553T=
XM_011520188.1:c.*553T= XP_011518490.1:n.*553T=
XM_011520189.1:c.*553T= XP_011518491.1:n.*553T=
XM_011520190.1:c.*768T= XP_011518492.1:n.*768T=
XM_006718253.3:c.*553T= XP_006718316.1:n.*553T=
XM_011520188.2:c.*553T= XP_011518490.1:n.*553T=
XM_011520189.2:c.*553T= XP_011518491.1:n.*553T=
XM_011520190.2:c.*768T= XP_011518492.1:n.*768T=
NM_001171968.2:c.*553T= NP_001165439.2:n.*553T=
NM_021924.5:c.*553T= MANE Select NP_068743.3:n.*553T=
NM_031264.4:c.*553T= NP_112554.3:n.*553T=
NM_001171968.3:c.*553T= NP_001165439.2:n.*553T=
NM_031264.5:c.*553T= NP_112554.3:n.*553T=