Canonical Allele Identifier: CA979830683
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs2074076453

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83493906_83493907insAA , CM000678.2:g.83493906_83493907insAA GRCh38
NC_000016.9:g.83527511_83527512insAA , CM000678.1:g.83527511_83527512insAA GRCh37
NC_000016.8:g.82085012_82085013insAA NCBI36
NG_052819.1:g.872113_872114insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000567109.6:c.960+7251_960+7252insAA MANE Select ENSP00000479395.1:n.960+7251_960+7252insAA
ENST00000268613.14:c.1101+7251_1101+7252insAA ENSP00000268613.10:n.1101+7251_1101+7252insAA
ENST00000428848.7:c.843+7251_843+7252insAA ENSP00000394557.3:n.843+7251_843+7252insAA
ENST00000539548.6:c.*592+7251_*592+7252insAA ENSP00000442225.2:n.*592+7251_*592+7252insAA
ENST00000566620.5:c.924+7251_924+7252insAA ENSP00000454435.3:n.924+7251_924+7252insAA
ENST00000567109.5:c.960+7251_960+7252insAA ENSP00000479395.1:n.960+7251_960+7252insAA
ENST00000622885.4:c.804+7251_804+7252insAA ENSP00000483719.1:n.804+7251_804+7252insAA
NM_001220488.1:c.1101+7251_1101+7252insAA NP_001207417.1:n.1101+7251_1101+7252insAA
NM_001220489.1:c.843+7251_843+7252insAA NP_001207418.1:n.843+7251_843+7252insAA
NM_001220490.1:c.198+7251_198+7252insAA NP_001207419.1:n.198+7251_198+7252insAA
NM_001257.4:c.960+7251_960+7252insAA NP_001248.1:n.960+7251_960+7252insAA
XM_011522804.1:c.657+7251_657+7252insAA XP_011521106.1:n.657+7251_657+7252insAA
XM_011522805.1:c.1101+7251_1101+7252insAA XP_011521107.1:n.1101+7251_1101+7252insAA
XM_011522804.3:c.657+7251_657+7252insAA XP_011521106.1:n.657+7251_657+7252insAA
XM_017022848.2:c.1101+7251_1101+7252insAA XP_016878337.1:n.1101+7251_1101+7252insAA
NM_001257.5:c.960+7251_960+7252insAA MANE Select NP_001248.1:n.960+7251_960+7252insAA
NM_001220488.2:c.1101+7251_1101+7252insAA NP_001207417.1:n.1101+7251_1101+7252insAA
NM_001220489.2:c.843+7251_843+7252insAA NP_001207418.1:n.843+7251_843+7252insAA
NM_001220490.2:c.198+7251_198+7252insAA NP_001207419.1:n.198+7251_198+7252insAA