Canonical Allele Identifier: CA14229941
Gene: CDH13 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6565113

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83074041G>T , CM000678.2:g.83074041G>T GRCh38
NC_000016.9:g.83107646G>T , CM000678.1:g.83107646G>T GRCh37
NC_000016.8:g.81665147G>T NCBI36
NG_052819.1:g.452248G>T

Transcript Alleles

HGVS Amino-acid change
NM_001220488.1:c.507+41823G>T VV NP_001207417.1:p.=
NM_001220489.1:c.366+41823G>T VV NP_001207418.1:p.=
NM_001220490.1:c.-396-51344G>T VV NP_001207419.1:p.=
NM_001220491.1:c.366+41823G>T VV NP_001207420.1:p.=
NM_001220492.1:c.366+41823G>T VV NP_001207421.1:p.=
NM_001257.4:c.366+41823G>T VV NP_001248.1:p.=
XM_011522804.1:c.63+5553G>T XP_011521106.1:p.=
XM_011522805.1:c.507+41823G>T XP_011521107.1:p.=
XM_011522804.3:c.63+5553G>T XP_011521106.1:p.=
XM_017022848.2:c.507+41823G>T XP_016878337.1:p.=
XM_017022849.2:c.507+41823G>T XP_016878338.1:p.=
NM_001257.5:c.366+41823G>T VV MANE Preferred NP_001248.1:p.=
ENST00000268613.14:c.507+41823G>T ENSP00000268613.10:p.=
ENST00000428848.7:c.366+41823G>T ENSP00000394557.3:p.=
ENST00000431540.7:c.366+41823G>T ENSP00000408632.3:p.=
ENST00000539548.6:c.158-51344G>T ENSP00000442225.2:p.=
ENST00000565636.5:c.366+41823G>T ENSP00000456491.1:p.=
ENST00000566620.5:n.330+41823G>T ENSP00000454435.3:p.=
ENST00000567109.5:c.366+41823G>T ENSP00000479395.1:p.=
ENST00000569454.1:n.283+41823G>T
ENST00000622885.4:n.327+41823G>T ENSP00000483719.1:p.=