Canonical Allele Identifier: CA2513221289
Gene: CDH13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83494002_83494003insCAAG , CM000678.2:g.83494002_83494003insCAAG GRCh38
NC_000016.9:g.83527607_83527608insCAAG , CM000678.1:g.83527607_83527608insCAAG GRCh37
NC_000016.8:g.82085108_82085109insCAAG NCBI36
NG_052819.1:g.872209_872210insCAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000567109.6:c.960+7347_960+7348insCAAG MANE Select ENSP00000479395.1:n.960+7347_960+7348insCAAG
ENST00000268613.14:c.1101+7347_1101+7348insCAAG ENSP00000268613.10:n.1101+7347_1101+7348insCAAG
ENST00000428848.7:c.843+7347_843+7348insCAAG ENSP00000394557.3:n.843+7347_843+7348insCAAG
ENST00000539548.6:c.*592+7347_*592+7348insCAAG ENSP00000442225.2:n.*592+7347_*592+7348insCAAG
ENST00000566620.5:c.924+7347_924+7348insCAAG ENSP00000454435.3:n.924+7347_924+7348insCAAG
ENST00000567109.5:c.960+7347_960+7348insCAAG ENSP00000479395.1:n.960+7347_960+7348insCAAG
ENST00000622885.4:c.804+7347_804+7348insCAAG ENSP00000483719.1:n.804+7347_804+7348insCAAG
NM_001220488.1:c.1101+7347_1101+7348insCAAG NP_001207417.1:n.1101+7347_1101+7348insCAAG
NM_001220489.1:c.843+7347_843+7348insCAAG NP_001207418.1:n.843+7347_843+7348insCAAG
NM_001220490.1:c.198+7347_198+7348insCAAG NP_001207419.1:n.198+7347_198+7348insCAAG
NM_001257.4:c.960+7347_960+7348insCAAG NP_001248.1:n.960+7347_960+7348insCAAG
XM_011522804.1:c.657+7347_657+7348insCAAG XP_011521106.1:n.657+7347_657+7348insCAAG
XM_011522805.1:c.1101+7347_1101+7348insCAAG XP_011521107.1:n.1101+7347_1101+7348insCAAG
XM_011522804.3:c.657+7347_657+7348insCAAG XP_011521106.1:n.657+7347_657+7348insCAAG
XM_017022848.2:c.1101+7347_1101+7348insCAAG XP_016878337.1:n.1101+7347_1101+7348insCAAG
NM_001257.5:c.960+7347_960+7348insCAAG MANE Select NP_001248.1:n.960+7347_960+7348insCAAG
NM_001220488.2:c.1101+7347_1101+7348insCAAG NP_001207417.1:n.1101+7347_1101+7348insCAAG
NM_001220489.2:c.843+7347_843+7348insCAAG NP_001207418.1:n.843+7347_843+7348insCAAG
NM_001220490.2:c.198+7347_198+7348insCAAG NP_001207419.1:n.198+7347_198+7348insCAAG