Canonical Allele Identifier: CA724954467
Gene: CDH13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83074041G>C , CM000678.2:g.83074041G>C GRCh38
NC_000016.9:g.83107646G>C , CM000678.1:g.83107646G>C GRCh37
NC_000016.8:g.81665147G>C NCBI36
NG_052819.1:g.452248G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000567109.6:c.366+41823G>C MANE Select ENSP00000479395.1:n.366+41823G>C
ENST00000268613.14:c.507+41823G>C ENSP00000268613.10:n.507+41823G>C
ENST00000428848.7:c.366+41823G>C ENSP00000394557.3:n.366+41823G>C
ENST00000431540.7:c.366+41823G>C ENSP00000408632.3:n.366+41823G>C
ENST00000539548.6:c.158-51344G>C ENSP00000442225.2:n.158-51344G>C
ENST00000565636.5:c.366+41823G>C ENSP00000456491.1:n.366+41823G>C
ENST00000566620.5:c.330+41823G>C ENSP00000454435.3:n.330+41823G>C
ENST00000567109.5:c.366+41823G>C ENSP00000479395.1:n.366+41823G>C
ENST00000569454.1:n.283+41823G>C
ENST00000622885.4:c.327+41823G>C ENSP00000483719.1:n.327+41823G>C
NM_001220488.1:c.507+41823G>C NP_001207417.1:n.507+41823G>C
NM_001220489.1:c.366+41823G>C NP_001207418.1:n.366+41823G>C
NM_001220490.1:c.-396-51344G>C NP_001207419.1:n.-396-51344G>C
NM_001220491.1:c.366+41823G>C NP_001207420.1:n.366+41823G>C
NM_001220492.1:c.366+41823G>C NP_001207421.1:n.366+41823G>C
NM_001257.4:c.366+41823G>C NP_001248.1:n.366+41823G>C
XM_011522804.1:c.63+5553G>C XP_011521106.1:n.63+5553G>C
XM_011522805.1:c.507+41823G>C XP_011521107.1:n.507+41823G>C
XM_011522804.3:c.63+5553G>C XP_011521106.1:n.63+5553G>C
XM_017022848.2:c.507+41823G>C XP_016878337.1:n.507+41823G>C
XM_017022849.2:c.507+41823G>C XP_016878338.1:n.507+41823G>C
NM_001257.5:c.366+41823G>C MANE Select NP_001248.1:n.366+41823G>C
NM_001220488.2:c.507+41823G>C NP_001207417.1:n.507+41823G>C
NM_001220489.2:c.366+41823G>C NP_001207418.1:n.366+41823G>C
NM_001220490.2:c.-396-51344G>C NP_001207419.1:n.-396-51344G>C
NM_001220491.2:c.366+41823G>C NP_001207420.1:n.366+41823G>C
NM_001220492.2:c.366+41823G>C NP_001207421.1:n.366+41823G>C
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