Canonical Allele Identifier: CA1947211178
Gene: CDHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.616936_616938delinsATC , CM000673.2:g.616936_616938delinsATC GRCh38
NC_000011.9:g.616936_616938delinsATC , CM000673.1:g.616936_616938delinsATC GRCh37
NC_000011.8:g.606936_606938delinsATC NCBI36
NG_029106.1:g.4062_4064delinsGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000358353.8:c.*413_*415delinsGAT ENSP00000351118.4:n.*413_*415delinsGAT
ENST00000397542.7:c.*413_*415delinsGAT MANE Select ENSP00000380676.2:n.*413_*415delinsGAT
ENST00000358353.7:c.*413_*415delinsGAT ENSP00000351118.3:n.*413_*415delinsGAT
ENST00000397542.6:c.*413_*415delinsGAT ENSP00000380676.2:n.*413_*415delinsGAT
NM_001171968.1:c.*413_*415delinsGAT NP_001165439.1:n.*413_*415delinsGAT
NM_021924.4:c.*413_*415delinsGAT NP_068743.2:n.*413_*415delinsGAT
NM_031264.3:c.*413_*415delinsGAT NP_112554.2:n.*413_*415delinsGAT
XM_006718253.2:c.*413_*415delinsGAT XP_006718316.1:n.*413_*415delinsGAT
XM_011520188.1:c.*413_*415delinsGAT XP_011518490.1:n.*413_*415delinsGAT
XM_011520189.1:c.*413_*415delinsGAT XP_011518491.1:n.*413_*415delinsGAT
XM_011520190.1:c.*628_*630delinsGAT XP_011518492.1:n.*628_*630delinsGAT
XM_006718253.3:c.*413_*415delinsGAT XP_006718316.1:n.*413_*415delinsGAT
XM_011520188.2:c.*413_*415delinsGAT XP_011518490.1:n.*413_*415delinsGAT
XM_011520189.2:c.*413_*415delinsGAT XP_011518491.1:n.*413_*415delinsGAT
XM_011520190.2:c.*628_*630delinsGAT XP_011518492.1:n.*628_*630delinsGAT
NM_001171968.2:c.*413_*415delinsGAT NP_001165439.2:n.*413_*415delinsGAT
NM_021924.5:c.*413_*415delinsGAT MANE Select NP_068743.3:n.*413_*415delinsGAT
NM_031264.4:c.*413_*415delinsGAT NP_112554.3:n.*413_*415delinsGAT
NM_001171968.3:c.*413_*415delinsGAT NP_001165439.2:n.*413_*415delinsGAT
NM_031264.5:c.*413_*415delinsGAT NP_112554.3:n.*413_*415delinsGAT