Canonical Allele Identifier: CA14230162
Gene: CDH13 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11644424

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83292454C>A , CM000678.2:g.83292454C>A GRCh38
NC_000016.9:g.83326059C>A , CM000678.1:g.83326059C>A GRCh37
NC_000016.8:g.81883560C>A NCBI36
NG_052819.1:g.670661C>A

Transcript Alleles

HGVS Amino-acid change
NM_001220488.1:c.778-52408C>A VV NP_001207417.1:p.=
NM_001220489.1:c.520-52408C>A VV NP_001207418.1:p.=
NM_001220490.1:c.-126-52408C>A VV NP_001207419.1:p.=
NM_001257.4:c.637-52408C>A VV NP_001248.1:p.=
XM_011522804.1:c.334-52408C>A XP_011521106.1:p.=
XM_011522805.1:c.778-52408C>A XP_011521107.1:p.=
XM_011522804.3:c.334-52408C>A
XM_017022848.2:c.778-52408C>A XP_016878337.1:p.=
ENST00000268613.14:c.778-52408C>A ENSP00000268613.10:p.=
ENST00000428848.7:c.520-52408C>A ENSP00000394557.3:p.=
ENST00000539548.6:c.*269-52408C>A ENSP00000442225.2:p.=
ENST00000566620.5:n.601-52408C>A ENSP00000454435.3:p.=
ENST00000567109.5:c.637-52408C>A ENSP00000479395.1:p.=
ENST00000569454.1:n.554-52408C>A
ENST00000622885.4:n.481-52408C>A ENSP00000483719.1:p.=