Canonical Allele Identifier: CA14288569
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs3784990

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83745465A>G , CM000678.2:g.83745465A>G GRCh38
NC_000016.9:g.83779070A>G , CM000678.1:g.83779070A>G GRCh37
NC_000016.8:g.82336571A>G NCBI36
NG_052819.1:g.1123672A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000567109.6:c.1539-2643A>G MANE Select ENSP00000479395.1:p.=
ENST00000268613.14:c.1680-2643A>G ENSP00000268613.10:p.=
ENST00000428848.7:c.1422-2643A>G ENSP00000394557.3:p.=
ENST00000539548.6:c.*1171-2643A>G ENSP00000442225.2:p.=
ENST00000566620.5:n.1503-2643A>G ENSP00000454435.3:p.=
ENST00000567109.5:c.1539-2643A>G ENSP00000479395.1:p.=
ENST00000615627.1:n.459-2643A>G ENSP00000482651.1:p.=
ENST00000622885.4:n.1383-2643A>G ENSP00000483719.1:p.=
NM_001220488.1:c.1680-2643A>G NP_001207417.1:p.=
NM_001220489.1:c.1422-2643A>G NP_001207418.1:p.=
NM_001220490.1:c.777-2643A>G NP_001207419.1:p.=
NM_001257.4:c.1539-2643A>G NP_001248.1:p.=
XM_011522804.1:c.1236-2643A>G XP_011521106.1:p.=
XM_011522804.3:c.1236-2643A>G XP_011521106.1:p.=
NM_001257.5:c.1539-2643A>G MANE Select NP_001248.1:p.=
NM_001220488.2:c.1680-2643A>G NP_001207417.1:p.=
NM_001220489.2:c.1422-2643A>G NP_001207418.1:p.=
NM_001220490.2:c.777-2643A>G NP_001207419.1:p.=