Canonical Allele Identifier: CA979828978
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs2072946224

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83453758_83453766del , CM000678.2:g.83453758_83453766del GRCh38
NC_000016.9:g.83487363_83487371del , CM000678.1:g.83487363_83487371del GRCh37
NC_000016.8:g.82044864_82044872del NCBI36
NG_052819.1:g.831965_831973del

Transcript Alleles

HGVS Amino-acid change
ENST00000567109.6:c.782-32719_782-32711del MANE Select ENSP00000479395.1:n.782-32719_782-32711de...
ENST00000268613.14:c.923-32719_923-32711del ENSP00000268613.10:n.923-32719_923-32711d...
ENST00000428848.7:c.665-32719_665-32711del ENSP00000394557.3:n.665-32719_665-32711de...
ENST00000539548.6:c.*414-32719_*414-32711del ENSP00000442225.2:n.*414-32719_*414-32711...
ENST00000566620.5:c.746-32719_746-32711del ENSP00000454435.3:n.746-32719_746-32711de...
ENST00000567109.5:c.782-32719_782-32711del ENSP00000479395.1:n.782-32719_782-32711de...
ENST00000569454.1:n.699-32719_699-32711del
ENST00000622885.4:c.626-32719_626-32711del ENSP00000483719.1:n.626-32719_626-32711de...
NM_001220488.1:c.923-32719_923-32711del NP_001207417.1:n.923-32719_923-32711del
NM_001220489.1:c.665-32719_665-32711del NP_001207418.1:n.665-32719_665-32711del
NM_001220490.1:c.20-32719_20-32711del NP_001207419.1:n.20-32719_20-32711del
NM_001257.4:c.782-32719_782-32711del NP_001248.1:n.782-32719_782-32711del
XM_011522804.1:c.479-32719_479-32711del XP_011521106.1:n.479-32719_479-32711del
XM_011522805.1:c.923-32719_923-32711del XP_011521107.1:n.923-32719_923-32711del
XM_011522804.3:c.479-32719_479-32711del XP_011521106.1:n.479-32719_479-32711del
XM_017022848.2:c.923-32719_923-32711del XP_016878337.1:n.923-32719_923-32711del
NM_001257.5:c.782-32719_782-32711del MANE Select NP_001248.1:n.782-32719_782-32711del
NM_001220488.2:c.923-32719_923-32711del NP_001207417.1:n.923-32719_923-32711del
NM_001220489.2:c.665-32719_665-32711del NP_001207418.1:n.665-32719_665-32711del
NM_001220490.2:c.20-32719_20-32711del NP_001207419.1:n.20-32719_20-32711del