Canonical Allele Identifier: CA724954349
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs1214423153

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83073858del , CM000678.2:g.83073858del GRCh38
NC_000016.9:g.83107463del , CM000678.1:g.83107463del GRCh37
NC_000016.8:g.81664964del NCBI36
NG_052819.1:g.452065del

Transcript Alleles

HGVS Amino-acid change
ENST00000567109.6:c.366+41640del MANE Select ENSP00000479395.1:n.366+41640del
ENST00000268613.14:c.507+41640del ENSP00000268613.10:n.507+41640del
ENST00000428848.7:c.366+41640del ENSP00000394557.3:n.366+41640del
ENST00000431540.7:c.366+41640del ENSP00000408632.3:n.366+41640del
ENST00000539548.6:c.158-51527del ENSP00000442225.2:n.158-51527del
ENST00000565636.5:c.366+41640del ENSP00000456491.1:n.366+41640del
ENST00000566620.5:c.330+41640del ENSP00000454435.3:n.330+41640del
ENST00000567109.5:c.366+41640del ENSP00000479395.1:n.366+41640del
ENST00000569454.1:n.283+41640del
ENST00000622885.4:c.327+41640del ENSP00000483719.1:n.327+41640del
NM_001220488.1:c.507+41640del NP_001207417.1:n.507+41640del
NM_001220489.1:c.366+41640del NP_001207418.1:n.366+41640del
NM_001220490.1:c.-396-51527del NP_001207419.1:n.-396-51527del
NM_001220491.1:c.366+41640del NP_001207420.1:n.366+41640del
NM_001220492.1:c.366+41640del NP_001207421.1:n.366+41640del
NM_001257.4:c.366+41640del NP_001248.1:n.366+41640del
XM_011522804.1:c.63+5370del XP_011521106.1:n.63+5370del
XM_011522805.1:c.507+41640del XP_011521107.1:n.507+41640del
XM_011522804.3:c.63+5370del XP_011521106.1:n.63+5370del
XM_017022848.2:c.507+41640del XP_016878337.1:n.507+41640del
XM_017022849.2:c.507+41640del XP_016878338.1:n.507+41640del
NM_001257.5:c.366+41640del MANE Select NP_001248.1:n.366+41640del
NM_001220488.2:c.507+41640del NP_001207417.1:n.507+41640del
NM_001220489.2:c.366+41640del NP_001207418.1:n.366+41640del
NM_001220490.2:c.-396-51527del NP_001207419.1:n.-396-51527del
NM_001220491.2:c.366+41640del NP_001207420.1:n.366+41640del
NM_001220492.2:c.366+41640del NP_001207421.1:n.366+41640del