Canonical Allele Identifier: CA2497411326

Gene: CDH13

Linked Data

• dbSNP Id: rs2072946757

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83453761_83453771del , CM000678.2:g.83453761_83453771del	GRCh38
NC_000016.9:g.83487366_83487376del , CM000678.1:g.83487366_83487376del	GRCh37
NC_000016.8:g.82044867_82044877del	NCBI36
NG_052819.1:g.831968_831978del

Transcript Alleles

HGVS	Amino-acid change
ENST00000567109.6:c.782-32716_782-32706del MANE Select	ENSP00000479395.1:n.782-32716_782-32706de...
ENST00000268613.14:c.923-32716_923-32706del	ENSP00000268613.10:n.923-32716_923-32706d...
ENST00000428848.7:c.665-32716_665-32706del	ENSP00000394557.3:n.665-32716_665-32706de...
ENST00000539548.6:c.*414-32716_*414-32706del	ENSP00000442225.2:n.*414-32716_*414-32706...
ENST00000566620.5:c.746-32716_746-32706del	ENSP00000454435.3:n.746-32716_746-32706de...
ENST00000567109.5:c.782-32716_782-32706del	ENSP00000479395.1:n.782-32716_782-32706de...
ENST00000569454.1:n.699-32716_699-32706del
ENST00000622885.4:c.626-32716_626-32706del	ENSP00000483719.1:n.626-32716_626-32706de...
NM_001220488.1:c.923-32716_923-32706del	NP_001207417.1:n.923-32716_923-32706del
NM_001220489.1:c.665-32716_665-32706del	NP_001207418.1:n.665-32716_665-32706del
NM_001220490.1:c.20-32716_20-32706del	NP_001207419.1:n.20-32716_20-32706del
NM_001257.4:c.782-32716_782-32706del	NP_001248.1:n.782-32716_782-32706del
XM_011522804.1:c.479-32716_479-32706del	XP_011521106.1:n.479-32716_479-32706del
XM_011522805.1:c.923-32716_923-32706del	XP_011521107.1:n.923-32716_923-32706del
XM_011522804.3:c.479-32716_479-32706del	XP_011521106.1:n.479-32716_479-32706del
XM_017022848.2:c.923-32716_923-32706del	XP_016878337.1:n.923-32716_923-32706del
NM_001257.5:c.782-32716_782-32706del MANE Select	NP_001248.1:n.782-32716_782-32706del
NM_001220488.2:c.923-32716_923-32706del	NP_001207417.1:n.923-32716_923-32706del
NM_001220489.2:c.665-32716_665-32706del	NP_001207418.1:n.665-32716_665-32706del
NM_001220490.2:c.20-32716_20-32706del	NP_001207419.1:n.20-32716_20-32706del