Canonical Allele Identifier: CA285855406
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs757816000

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83292631_83292633del , CM000678.2:g.83292631_83292633del GRCh38
NC_000016.9:g.83326236_83326238del , CM000678.1:g.83326236_83326238del GRCh37
NC_000016.8:g.81883737_81883739del NCBI36
NG_052819.1:g.670838_670840del

Transcript Alleles

HGVS Amino-acid Change
ENST00000567109.6:c.637-52231_637-52229del MANE Select ENSP00000479395.1:n.637-52231_637-52229del
ENST00000268613.14:c.778-52231_778-52229del ENSP00000268613.10:n.778-52231_778-52229del
ENST00000428848.7:c.520-52231_520-52229del ENSP00000394557.3:n.520-52231_520-52229del
ENST00000539548.6:c.*269-52231_*269-52229del ENSP00000442225.2:n.*269-52231_*269-52229del
ENST00000566620.5:c.601-52231_601-52229del ENSP00000454435.3:n.601-52231_601-52229del
ENST00000567109.5:c.637-52231_637-52229del ENSP00000479395.1:n.637-52231_637-52229del
ENST00000569454.1:n.554-52231_554-52229del
ENST00000622885.4:c.481-52231_481-52229del ENSP00000483719.1:n.481-52231_481-52229del
NM_001220488.1:c.778-52231_778-52229del NP_001207417.1:n.778-52231_778-52229del
NM_001220489.1:c.520-52231_520-52229del NP_001207418.1:n.520-52231_520-52229del
NM_001220490.1:c.-126-52231_-126-52229del NP_001207419.1:n.-126-52231_-126-52229del
NM_001257.4:c.637-52231_637-52229del NP_001248.1:n.637-52231_637-52229del
XM_011522804.1:c.334-52231_334-52229del XP_011521106.1:n.334-52231_334-52229del
XM_011522805.1:c.778-52231_778-52229del XP_011521107.1:n.778-52231_778-52229del
XM_011522804.3:c.334-52231_334-52229del XP_011521106.1:n.334-52231_334-52229del
XM_017022848.2:c.778-52231_778-52229del XP_016878337.1:n.778-52231_778-52229del
NM_001257.5:c.637-52231_637-52229del MANE Select NP_001248.1:n.637-52231_637-52229del
NM_001220488.2:c.778-52231_778-52229del NP_001207417.1:n.778-52231_778-52229del
NM_001220489.2:c.520-52231_520-52229del NP_001207418.1:n.520-52231_520-52229del
NM_001220490.2:c.-126-52231_-126-52229del NP_001207419.1:n.-126-52231_-126-52229del