Canonical Allele Identifier: CA285855380
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs1039316273

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83292499C>T , CM000678.2:g.83292499C>T GRCh38
NC_000016.9:g.83326104C>T , CM000678.1:g.83326104C>T GRCh37
NC_000016.8:g.81883605C>T NCBI36
NG_052819.1:g.670706C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000567109.6:c.637-52363C>T MANE Select ENSP00000479395.1:n.637-52363C>T
ENST00000268613.14:c.778-52363C>T ENSP00000268613.10:n.778-52363C>T
ENST00000428848.7:c.520-52363C>T ENSP00000394557.3:n.520-52363C>T
ENST00000539548.6:c.*269-52363C>T ENSP00000442225.2:n.*269-52363C>T
ENST00000566620.5:c.601-52363C>T ENSP00000454435.3:n.601-52363C>T
ENST00000567109.5:c.637-52363C>T ENSP00000479395.1:n.637-52363C>T
ENST00000569454.1:n.554-52363C>T
ENST00000622885.4:c.481-52363C>T ENSP00000483719.1:n.481-52363C>T
NM_001220488.1:c.778-52363C>T NP_001207417.1:n.778-52363C>T
NM_001220489.1:c.520-52363C>T NP_001207418.1:n.520-52363C>T
NM_001220490.1:c.-126-52363C>T NP_001207419.1:n.-126-52363C>T
NM_001257.4:c.637-52363C>T NP_001248.1:n.637-52363C>T
XM_011522804.1:c.334-52363C>T XP_011521106.1:n.334-52363C>T
XM_011522805.1:c.778-52363C>T XP_011521107.1:n.778-52363C>T
XM_011522804.3:c.334-52363C>T XP_011521106.1:n.334-52363C>T
XM_017022848.2:c.778-52363C>T XP_016878337.1:n.778-52363C>T
NM_001257.5:c.637-52363C>T MANE Select NP_001248.1:n.637-52363C>T
NM_001220488.2:c.778-52363C>T NP_001207417.1:n.778-52363C>T
NM_001220489.2:c.520-52363C>T NP_001207418.1:n.520-52363C>T
NM_001220490.2:c.-126-52363C>T NP_001207419.1:n.-126-52363C>T