Canonical Allele Identifier: CA396194334
Gene: CDH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66398531G>T , CM000678.2:g.66398531G>T GRCh38
NC_000016.9:g.66432434G>T , CM000678.1:g.66432434G>T GRCh37
NC_000016.8:g.64989935G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000341529.8:c.1561G>T MANE Select ENSP00000344115.3:p.Glu521Ter
ENST00000649567.1:c.1561G>T ENSP00000497290.1:p.Glu521Ter
ENST00000341529.7:c.1561G>T ENSP00000344115.3:p.Glu521Ter
ENST00000539168.1:c.-123G>T ENSP00000461880.1:n.-123G>T
ENST00000565334.5:c.*684G>T ENSP00000456028.1:n.*684G>T
ENST00000614547.4:c.1216G>T ENSP00000479381.1:p.Glu406Ter
NM_001795.3:c.1561G>T NP_001786.2:p.Glu521Ter
XM_011522801.1:c.1588G>T XP_011521103.1:p.Glu530Ter
NM_001795.4:c.1561G>T NP_001786.2:p.Glu521Ter
XM_011522801.2:c.1588G>T XP_011521103.1:p.Glu530Ter
XM_024450133.1:c.1588G>T XP_024305901.1:p.Glu530Ter
NM_001795.5:c.1561G>T MANE Select NP_001786.2:p.Glu521Ter