Canonical Allele Identifier: CA724871420
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs1310122418

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82783975dup , CM000678.2:g.82783975dup GRCh38
NC_000016.9:g.82817580dup , CM000678.1:g.82817580dup GRCh37
NC_000016.8:g.81375081dup NCBI36
NG_052819.1:g.162182dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000567109.6:c.46-74387dup MANE Select ENSP00000479395.1:n.46-74387dup
ENST00000268613.14:c.187-74387dup ENSP00000268613.10:n.187-74387dup
ENST00000428848.7:c.46-74387dup ENSP00000394557.3:n.46-74387dup
ENST00000431540.7:c.46-74387dup ENSP00000408632.3:n.46-74387dup
ENST00000539548.6:c.46-74387dup ENSP00000442225.2:n.46-74387dup
ENST00000562601.5:c.*55-74387dup ENSP00000455781.1:n.*55-74387dup
ENST00000565636.5:c.46-74387dup ENSP00000456491.1:n.46-74387dup
ENST00000566333.1:n.168-74387dup
ENST00000567109.5:c.46-74387dup ENSP00000479395.1:n.46-74387dup
ENST00000567445.1:c.46-74387dup ENSP00000456297.1:n.46-74387dup
ENST00000568770.5:c.*45+64500dup ENSP00000457149.1:n.*45+64500dup
ENST00000569144.5:c.46-74387dup ENSP00000457914.1:n.46-74387dup
NM_001220488.1:c.187-74387dup NP_001207417.1:n.187-74387dup
NM_001220489.1:c.46-74387dup NP_001207418.1:n.46-74387dup
NM_001220490.1:c.-508-74387dup NP_001207419.1:n.-508-74387dup
NM_001220491.1:c.46-74387dup NP_001207420.1:n.46-74387dup
NM_001220492.1:c.46-74387dup NP_001207421.1:n.46-74387dup
NM_001257.4:c.46-74387dup NP_001248.1:n.46-74387dup
NR_110938.1:n.171+10486dup
XM_011522805.1:c.187-74387dup XP_011521107.1:n.187-74387dup
XM_017022848.2:c.187-74387dup XP_016878337.1:n.187-74387dup
XM_017022849.2:c.187-74387dup XP_016878338.1:n.187-74387dup
NM_001257.5:c.46-74387dup MANE Select NP_001248.1:n.46-74387dup
NM_001220488.2:c.187-74387dup NP_001207417.1:n.187-74387dup
NM_001220489.2:c.46-74387dup NP_001207418.1:n.46-74387dup
NM_001220490.2:c.-508-74387dup NP_001207419.1:n.-508-74387dup
NM_001220491.2:c.46-74387dup NP_001207420.1:n.46-74387dup
NM_001220492.2:c.46-74387dup NP_001207421.1:n.46-74387dup