Canonical Allele Identifier: CA2228852428
Community Standard Title: NM_001795.5(CDH5):c.1550T= (p.Ile517=)
Gene: CDH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66398520T= , CM000678.2:g.66398520T= GRCh38
NC_000016.9:g.66432423T= , CM000678.1:g.66432423T= GRCh37
NC_000016.8:g.64989924T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001795.5:c.1550T= MANE Select NP_001786.2:p.Ile517=
ENST00000341529.8:c.1550T= MANE Select ENSP00000344115.3:p.Ile517=
NM_001795.3:c.1550T= NP_001786.2:p.Ile517=
NM_001795.4:c.1550T= NP_001786.2:p.Ile517=
ENST00000341529.7:c.1550T= ENSP00000344115.3:p.Ile517=
ENST00000539168.1:c.-134T= ENSP00000461880.1:n.-134T=
ENST00000565334.5:c.*673T= ENSP00000456028.1:n.*673T=
ENST00000614547.4:c.1205T= ENSP00000479381.1:p.Ile402=
ENST00000649567.1:c.1550T= ENSP00000497290.1:p.Ile517=
XM_011522801.1:c.1577T= XP_011521103.1:p.Ile526=
XM_011522801.2:c.1577T= XP_011521103.1:p.Ile526=
XM_024450133.1:c.1577T= XP_024305901.1:p.Ile526=