Canonical Allele Identifier: CA979811702
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs2040172375

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83237235_83237236del , CM000678.2:g.83237235_83237236del GRCh38
NC_000016.9:g.83270840_83270841del , CM000678.1:g.83270840_83270841del GRCh37
NC_000016.8:g.81828341_81828342del NCBI36
NG_052819.1:g.615442_615443del

Transcript Alleles

HGVS Amino-acid Change
ENST00000567109.6:c.636+19738_636+19739del MANE Select ENSP00000479395.1:n.636+19738_636+19739del
ENST00000268613.14:c.777+19738_777+19739del ENSP00000268613.10:n.777+19738_777+19739del
ENST00000428848.7:c.519+19738_519+19739del ENSP00000394557.3:n.519+19738_519+19739del
ENST00000539548.6:c.*268+19738_*268+19739del ENSP00000442225.2:n.*268+19738_*268+19739del
ENST00000566620.5:c.600+19738_600+19739del ENSP00000454435.3:n.600+19738_600+19739del
ENST00000567109.5:c.636+19738_636+19739del ENSP00000479395.1:n.636+19738_636+19739del
ENST00000569454.1:n.553+19738_553+19739del
ENST00000622885.4:c.480+19738_480+19739del ENSP00000483719.1:n.480+19738_480+19739del
NM_001220488.1:c.777+19738_777+19739del NP_001207417.1:n.777+19738_777+19739del
NM_001220489.1:c.519+19738_519+19739del NP_001207418.1:n.519+19738_519+19739del
NM_001220490.1:c.-127+19738_-127+19739del NP_001207419.1:n.-127+19738_-127+19739del
NM_001257.4:c.636+19738_636+19739del NP_001248.1:n.636+19738_636+19739del
XM_011522804.1:c.333+19738_333+19739del XP_011521106.1:n.333+19738_333+19739del
XM_011522805.1:c.777+19738_777+19739del XP_011521107.1:n.777+19738_777+19739del
XM_011522804.3:c.333+19738_333+19739del XP_011521106.1:n.333+19738_333+19739del
XM_017022848.2:c.777+19738_777+19739del XP_016878337.1:n.777+19738_777+19739del
NM_001257.5:c.636+19738_636+19739del MANE Select NP_001248.1:n.636+19738_636+19739del
NM_001220488.2:c.777+19738_777+19739del NP_001207417.1:n.777+19738_777+19739del
NM_001220489.2:c.519+19738_519+19739del NP_001207418.1:n.519+19738_519+19739del
NM_001220490.2:c.-127+19738_-127+19739del NP_001207419.1:n.-127+19738_-127+19739del