Canonical Allele Identifier: CA2237939143

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82783843_82783845delinsGCT , CM000678.2:g.82783843_82783845delinsGCT	GRCh38
NC_000016.9:g.82817448_82817450delinsGCT , CM000678.1:g.82817448_82817450delinsGCT	GRCh37
NC_000016.8:g.81374949_81374951delinsGCT	NCBI36
NG_052819.1:g.162050_162052delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567109.6:c.46-74519_46-74517delinsGCT MANE Select	ENSP00000479395.1:n.46-74519_46-74517delinsGCT
ENST00000268613.14:c.187-74519_187-74517delinsGCT	ENSP00000268613.10:n.187-74519_187-74517delinsGCT
ENST00000428848.7:c.46-74519_46-74517delinsGCT	ENSP00000394557.3:n.46-74519_46-74517delinsGCT
ENST00000431540.7:c.46-74519_46-74517delinsGCT	ENSP00000408632.3:n.46-74519_46-74517delinsGCT
ENST00000539548.6:c.46-74519_46-74517delinsGCT	ENSP00000442225.2:n.46-74519_46-74517delinsGCT
ENST00000562601.5:c.*55-74519_*55-74517delinsGCT	ENSP00000455781.1:n.*55-74519_*55-74517delinsGCT
ENST00000565636.5:c.46-74519_46-74517delinsGCT	ENSP00000456491.1:n.46-74519_46-74517delinsGCT
ENST00000566333.1:n.168-74519_168-74517delinsGCT
ENST00000567109.5:c.46-74519_46-74517delinsGCT	ENSP00000479395.1:n.46-74519_46-74517delinsGCT
ENST00000567445.1:c.46-74519_46-74517delinsGCT	ENSP00000456297.1:n.46-74519_46-74517delinsGCT
ENST00000568770.5:c.*45+64368_*45+64370delinsGCT	ENSP00000457149.1:n.*45+64368_*45+64370delinsGCT
ENST00000569144.5:c.46-74519_46-74517delinsGCT	ENSP00000457914.1:n.46-74519_46-74517delinsGCT
NM_001220488.1:c.187-74519_187-74517delinsGCT	NP_001207417.1:n.187-74519_187-74517delinsGCT
NM_001220489.1:c.46-74519_46-74517delinsGCT	NP_001207418.1:n.46-74519_46-74517delinsGCT
NM_001220490.1:c.-508-74519_-508-74517delinsGCT	NP_001207419.1:n.-508-74519_-508-74517delinsGCT
NM_001220491.1:c.46-74519_46-74517delinsGCT	NP_001207420.1:n.46-74519_46-74517delinsGCT
NM_001220492.1:c.46-74519_46-74517delinsGCT	NP_001207421.1:n.46-74519_46-74517delinsGCT
NM_001257.4:c.46-74519_46-74517delinsGCT	NP_001248.1:n.46-74519_46-74517delinsGCT
NR_110938.1:n.171+10354_171+10356delinsGCT
XM_011522805.1:c.187-74519_187-74517delinsGCT	XP_011521107.1:n.187-74519_187-74517delinsGCT
XM_017022848.2:c.187-74519_187-74517delinsGCT	XP_016878337.1:n.187-74519_187-74517delinsGCT
XM_017022849.2:c.187-74519_187-74517delinsGCT	XP_016878338.1:n.187-74519_187-74517delinsGCT
NM_001257.5:c.46-74519_46-74517delinsGCT MANE Select	NP_001248.1:n.46-74519_46-74517delinsGCT
NM_001220488.2:c.187-74519_187-74517delinsGCT	NP_001207417.1:n.187-74519_187-74517delinsGCT
NM_001220489.2:c.46-74519_46-74517delinsGCT	NP_001207418.1:n.46-74519_46-74517delinsGCT
NM_001220490.2:c.-508-74519_-508-74517delinsGCT	NP_001207419.1:n.-508-74519_-508-74517delinsGCT
NM_001220491.2:c.46-74519_46-74517delinsGCT	NP_001207420.1:n.46-74519_46-74517delinsGCT
NM_001220492.2:c.46-74519_46-74517delinsGCT	NP_001207421.1:n.46-74519_46-74517delinsGCT