Canonical Allele Identifier: CA979828993
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs2072947470

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83453769_83453772del , CM000678.2:g.83453769_83453772del GRCh38
NC_000016.9:g.83487374_83487377del , CM000678.1:g.83487374_83487377del GRCh37
NC_000016.8:g.82044875_82044878del NCBI36
NG_052819.1:g.831976_831979del

Transcript Alleles

HGVS Amino-acid change
ENST00000567109.6:c.782-32708_782-32705del MANE Select ENSP00000479395.1:n.782-32708_782-32705de...
ENST00000268613.14:c.923-32708_923-32705del ENSP00000268613.10:n.923-32708_923-32705d...
ENST00000428848.7:c.665-32708_665-32705del ENSP00000394557.3:n.665-32708_665-32705de...
ENST00000539548.6:c.*414-32708_*414-32705del ENSP00000442225.2:n.*414-32708_*414-32705...
ENST00000566620.5:c.746-32708_746-32705del ENSP00000454435.3:n.746-32708_746-32705de...
ENST00000567109.5:c.782-32708_782-32705del ENSP00000479395.1:n.782-32708_782-32705de...
ENST00000569454.1:n.699-32708_699-32705del
ENST00000622885.4:c.626-32708_626-32705del ENSP00000483719.1:n.626-32708_626-32705de...
NM_001220488.1:c.923-32708_923-32705del NP_001207417.1:n.923-32708_923-32705del
NM_001220489.1:c.665-32708_665-32705del NP_001207418.1:n.665-32708_665-32705del
NM_001220490.1:c.20-32708_20-32705del NP_001207419.1:n.20-32708_20-32705del
NM_001257.4:c.782-32708_782-32705del NP_001248.1:n.782-32708_782-32705del
XM_011522804.1:c.479-32708_479-32705del XP_011521106.1:n.479-32708_479-32705del
XM_011522805.1:c.923-32708_923-32705del XP_011521107.1:n.923-32708_923-32705del
XM_011522804.3:c.479-32708_479-32705del XP_011521106.1:n.479-32708_479-32705del
XM_017022848.2:c.923-32708_923-32705del XP_016878337.1:n.923-32708_923-32705del
NM_001257.5:c.782-32708_782-32705del MANE Select NP_001248.1:n.782-32708_782-32705del
NM_001220488.2:c.923-32708_923-32705del NP_001207417.1:n.923-32708_923-32705del
NM_001220489.2:c.665-32708_665-32705del NP_001207418.1:n.665-32708_665-32705del
NM_001220490.2:c.20-32708_20-32705del NP_001207419.1:n.20-32708_20-32705del