Canonical Allele Identifier: CA14288499
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs6563943

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83605730G>A , CM000678.2:g.83605730G>A GRCh38
NC_000016.9:g.83639335G>A , CM000678.1:g.83639335G>A GRCh37
NC_000016.8:g.82196836G>A NCBI36
NG_052819.1:g.983937G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000567109.6:c.1101+3136G>A MANE Select ENSP00000479395.1:p.=
ENST00000268613.14:c.1242+3136G>A ENSP00000268613.10:p.=
ENST00000428848.7:c.984+3136G>A ENSP00000394557.3:p.=
ENST00000539548.6:c.*733+3136G>A ENSP00000442225.2:p.=
ENST00000566620.5:n.1065+3136G>A ENSP00000454435.3:p.=
ENST00000567109.5:c.1101+3136G>A ENSP00000479395.1:p.=
ENST00000622885.4:n.945+3136G>A ENSP00000483719.1:p.=
NM_001220488.1:c.1242+3136G>A NP_001207417.1:p.=
NM_001220489.1:c.984+3136G>A NP_001207418.1:p.=
NM_001220490.1:c.339+3136G>A NP_001207419.1:p.=
NM_001257.4:c.1101+3136G>A NP_001248.1:p.=
XM_011522804.1:c.798+3136G>A XP_011521106.1:p.=
XM_011522805.1:c.1242+3136G>A XP_011521107.1:p.=
XM_011522804.3:c.798+3136G>A XP_011521106.1:p.=
NM_001257.5:c.1101+3136G>A MANE Select NP_001248.1:p.=
NM_001220488.2:c.1242+3136G>A NP_001207417.1:p.=
NM_001220489.2:c.984+3136G>A NP_001207418.1:p.=
NM_001220490.2:c.339+3136G>A NP_001207419.1:p.=