Canonical Allele Identifier: CA979828979
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs2072946292

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83453756_83453767del , CM000678.2:g.83453756_83453767del GRCh38
NC_000016.9:g.83487361_83487372del , CM000678.1:g.83487361_83487372del GRCh37
NC_000016.8:g.82044862_82044873del NCBI36
NG_052819.1:g.831963_831974del

Transcript Alleles

HGVS Amino-acid change
ENST00000567109.6:c.782-32721_782-32710del MANE Select ENSP00000479395.1:n.782-32721_782-32710de...
ENST00000268613.14:c.923-32721_923-32710del ENSP00000268613.10:n.923-32721_923-32710d...
ENST00000428848.7:c.665-32721_665-32710del ENSP00000394557.3:n.665-32721_665-32710de...
ENST00000539548.6:c.*414-32721_*414-32710del ENSP00000442225.2:n.*414-32721_*414-32710...
ENST00000566620.5:c.746-32721_746-32710del ENSP00000454435.3:n.746-32721_746-32710de...
ENST00000567109.5:c.782-32721_782-32710del ENSP00000479395.1:n.782-32721_782-32710de...
ENST00000569454.1:n.699-32721_699-32710del
ENST00000622885.4:c.626-32721_626-32710del ENSP00000483719.1:n.626-32721_626-32710de...
NM_001220488.1:c.923-32721_923-32710del NP_001207417.1:n.923-32721_923-32710del
NM_001220489.1:c.665-32721_665-32710del NP_001207418.1:n.665-32721_665-32710del
NM_001220490.1:c.20-32721_20-32710del NP_001207419.1:n.20-32721_20-32710del
NM_001257.4:c.782-32721_782-32710del NP_001248.1:n.782-32721_782-32710del
XM_011522804.1:c.479-32721_479-32710del XP_011521106.1:n.479-32721_479-32710del
XM_011522805.1:c.923-32721_923-32710del XP_011521107.1:n.923-32721_923-32710del
XM_011522804.3:c.479-32721_479-32710del XP_011521106.1:n.479-32721_479-32710del
XM_017022848.2:c.923-32721_923-32710del XP_016878337.1:n.923-32721_923-32710del
NM_001257.5:c.782-32721_782-32710del MANE Select NP_001248.1:n.782-32721_782-32710del
NM_001220488.2:c.923-32721_923-32710del NP_001207417.1:n.923-32721_923-32710del
NM_001220489.2:c.665-32721_665-32710del NP_001207418.1:n.665-32721_665-32710del
NM_001220490.2:c.20-32721_20-32710del NP_001207419.1:n.20-32721_20-32710del