Canonical Allele Identifier: CA919754390
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs1567529990

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82783827_82783828insC , CM000678.2:g.82783827_82783828insC GRCh38
NC_000016.9:g.82817432_82817433insC , CM000678.1:g.82817432_82817433insC GRCh37
NC_000016.8:g.81374933_81374934insC NCBI36
NG_052819.1:g.162034_162035insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000567109.6:c.46-74535_46-74534insC MANE Select ENSP00000479395.1:n.46-74535_46-74534insC
ENST00000268613.14:c.187-74535_187-74534insC ENSP00000268613.10:n.187-74535_187-74534insC
ENST00000428848.7:c.46-74535_46-74534insC ENSP00000394557.3:n.46-74535_46-74534insC
ENST00000431540.7:c.46-74535_46-74534insC ENSP00000408632.3:n.46-74535_46-74534insC
ENST00000539548.6:c.46-74535_46-74534insC ENSP00000442225.2:n.46-74535_46-74534insC
ENST00000562601.5:c.*55-74535_*55-74534insC ENSP00000455781.1:n.*55-74535_*55-74534insC
ENST00000565636.5:c.46-74535_46-74534insC ENSP00000456491.1:n.46-74535_46-74534insC
ENST00000566333.1:n.168-74535_168-74534insC
ENST00000567109.5:c.46-74535_46-74534insC ENSP00000479395.1:n.46-74535_46-74534insC
ENST00000567445.1:c.46-74535_46-74534insC ENSP00000456297.1:n.46-74535_46-74534insC
ENST00000568770.5:c.*45+64352_*45+64353insC ENSP00000457149.1:n.*45+64352_*45+64353insC
ENST00000569144.5:c.46-74535_46-74534insC ENSP00000457914.1:n.46-74535_46-74534insC
NM_001220488.1:c.187-74535_187-74534insC NP_001207417.1:n.187-74535_187-74534insC
NM_001220489.1:c.46-74535_46-74534insC NP_001207418.1:n.46-74535_46-74534insC
NM_001220490.1:c.-508-74535_-508-74534insC NP_001207419.1:n.-508-74535_-508-74534insC
NM_001220491.1:c.46-74535_46-74534insC NP_001207420.1:n.46-74535_46-74534insC
NM_001220492.1:c.46-74535_46-74534insC NP_001207421.1:n.46-74535_46-74534insC
NM_001257.4:c.46-74535_46-74534insC NP_001248.1:n.46-74535_46-74534insC
NR_110938.1:n.171+10338_171+10339insC
XM_011522805.1:c.187-74535_187-74534insC XP_011521107.1:n.187-74535_187-74534insC
XM_017022848.2:c.187-74535_187-74534insC XP_016878337.1:n.187-74535_187-74534insC
XM_017022849.2:c.187-74535_187-74534insC XP_016878338.1:n.187-74535_187-74534insC
NM_001257.5:c.46-74535_46-74534insC MANE Select NP_001248.1:n.46-74535_46-74534insC
NM_001220488.2:c.187-74535_187-74534insC NP_001207417.1:n.187-74535_187-74534insC
NM_001220489.2:c.46-74535_46-74534insC NP_001207418.1:n.46-74535_46-74534insC
NM_001220490.2:c.-508-74535_-508-74534insC NP_001207419.1:n.-508-74535_-508-74534insC
NM_001220491.2:c.46-74535_46-74534insC NP_001207420.1:n.46-74535_46-74534insC
NM_001220492.2:c.46-74535_46-74534insC NP_001207421.1:n.46-74535_46-74534insC