Canonical Allele Identifier: CA2228852337
Gene: CDH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66398420_66398421delinsAC , CM000678.2:g.66398420_66398421delinsAC GRCh38
NC_000016.9:g.66432323_66432324delinsAC , CM000678.1:g.66432323_66432324delinsAC GRCh37
NC_000016.8:g.64989824_64989825delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000341529.8:c.1486-36_1486-35delinsAC MANE Select ENSP00000344115.3:n.1486-36_1486-35delins...
ENST00000649567.1:c.1486-36_1486-35delinsAC ENSP00000497290.1:n.1486-36_1486-35delins...
ENST00000341529.7:c.1486-36_1486-35delinsAC ENSP00000344115.3:n.1486-36_1486-35delins...
ENST00000539168.1:c.-198-36_-198-35delinsAC ENSP00000461880.1:n.-198-36_-198-35delins...
ENST00000565334.5:c.*609-36_*609-35delinsAC ENSP00000456028.1:n.*609-36_*609-35delins...
ENST00000614547.4:c.1141-36_1141-35delinsAC ENSP00000479381.1:n.1141-36_1141-35delins...
NM_001795.3:c.1486-36_1486-35delinsAC NP_001786.2:n.1486-36_1486-35delinsAC
XM_011522801.1:c.1513-36_1513-35delinsAC XP_011521103.1:n.1513-36_1513-35delinsAC
NM_001795.4:c.1486-36_1486-35delinsAC NP_001786.2:n.1486-36_1486-35delinsAC
XM_011522801.2:c.1513-36_1513-35delinsAC XP_011521103.1:n.1513-36_1513-35delinsAC
XM_024450133.1:c.1513-36_1513-35delinsAC XP_024305901.1:n.1513-36_1513-35delinsAC
NM_001795.5:c.1486-36_1486-35delinsAC MANE Select NP_001786.2:n.1486-36_1486-35delinsAC