Canonical Allele Identifier: CA15887241
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs8058532

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83676061C>T , CM000678.2:g.83676061C>T GRCh38
NC_000016.9:g.83709666C>T , CM000678.1:g.83709666C>T GRCh37
NC_000016.8:g.82267167C>T NCBI36
NG_052819.1:g.1054268C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000567109.6:c.1285-2147C>T MANE Select ENSP00000479395.1:p.=
ENST00000268613.14:c.1426-2147C>T ENSP00000268613.10:p.=
ENST00000428848.7:c.1168-2147C>T ENSP00000394557.3:p.=
ENST00000539548.6:c.*917-2147C>T ENSP00000442225.2:p.=
ENST00000566620.5:n.1249-2147C>T ENSP00000454435.3:p.=
ENST00000567109.5:c.1285-2147C>T ENSP00000479395.1:p.=
ENST00000615627.1:n.205-2147C>T ENSP00000482651.1:p.=
ENST00000622885.4:n.1129-2147C>T ENSP00000483719.1:p.=
NM_001220488.1:c.1426-2147C>T NP_001207417.1:p.=
NM_001220489.1:c.1168-2147C>T NP_001207418.1:p.=
NM_001220490.1:c.523-2147C>T NP_001207419.1:p.=
NM_001257.4:c.1285-2147C>T NP_001248.1:p.=
XM_011522804.1:c.982-2147C>T XP_011521106.1:p.=
XM_011522804.3:c.982-2147C>T XP_011521106.1:p.=
XR_001752385.2:n.6466-8470G>A
NM_001257.5:c.1285-2147C>T MANE Select NP_001248.1:p.=
NM_001220488.2:c.1426-2147C>T NP_001207417.1:p.=
NM_001220489.2:c.1168-2147C>T NP_001207418.1:p.=
NM_001220490.2:c.523-2147C>T NP_001207419.1:p.=