Canonical Allele Identifier: CA8093104
Gene: CDH5 HGNC NCBI

Linked Data

dbSNP Id: rs1049970

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000341529.8:c.1550T>C MANE Select ENSP00000344115.3:p.Ile517Thr
ENST00000649567.1:c.1550T>C ENSP00000497290.1:p.Ile517Thr
ENST00000341529.7:c.1550T>C ENSP00000344115.3:p.Ile517Thr
ENST00000539168.1:c.-134T>C ENSP00000461880.1:n.-134T>C
ENST00000565334.5:c.*673T>C ENSP00000456028.1:n.*673T>C
ENST00000614547.4:c.1205T>C ENSP00000479381.1:p.Ile402Thr
NM_001795.3:c.1550T>C NP_001786.2:p.Ile517Thr
XM_011522801.1:c.1577T>C XP_011521103.1:p.Ile526Thr
NM_001795.4:c.1550T>C NP_001786.2:p.Ile517Thr
XM_011522801.2:c.1577T>C XP_011521103.1:p.Ile526Thr
XM_024450133.1:c.1577T>C XP_024305901.1:p.Ile526Thr
NM_001795.5:c.1550T>C MANE Select NP_001786.2:p.Ile517Thr