Canonical Allele Identifier: CA2237938665

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82783802_82783805delinsAGGC , CM000678.2:g.82783802_82783805delinsAGGC	GRCh38
NC_000016.9:g.82817407_82817410delinsAGGC , CM000678.1:g.82817407_82817410delinsAGGC	GRCh37
NC_000016.8:g.81374908_81374911delinsAGGC	NCBI36
NG_052819.1:g.162009_162012delinsAGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567109.6:c.46-74560_46-74557delinsAGGC MANE Select	ENSP00000479395.1:n.46-74560_46-74557delinsAGGC
ENST00000268613.14:c.187-74560_187-74557delinsAGGC	ENSP00000268613.10:n.187-74560_187-74557delinsAGGC
ENST00000428848.7:c.46-74560_46-74557delinsAGGC	ENSP00000394557.3:n.46-74560_46-74557delinsAGGC
ENST00000431540.7:c.46-74560_46-74557delinsAGGC	ENSP00000408632.3:n.46-74560_46-74557delinsAGGC
ENST00000539548.6:c.46-74560_46-74557delinsAGGC	ENSP00000442225.2:n.46-74560_46-74557delinsAGGC
ENST00000562601.5:c.*55-74560_*55-74557delinsAGGC	ENSP00000455781.1:n.*55-74560_*55-74557delinsAGGC
ENST00000565636.5:c.46-74560_46-74557delinsAGGC	ENSP00000456491.1:n.46-74560_46-74557delinsAGGC
ENST00000566333.1:n.168-74560_168-74557delinsAGGC
ENST00000567109.5:c.46-74560_46-74557delinsAGGC	ENSP00000479395.1:n.46-74560_46-74557delinsAGGC
ENST00000567445.1:c.46-74560_46-74557delinsAGGC	ENSP00000456297.1:n.46-74560_46-74557delinsAGGC
ENST00000568770.5:c.*45+64327_*45+64330delinsAGGC	ENSP00000457149.1:n.*45+64327_*45+64330delinsAGGC
ENST00000569144.5:c.46-74560_46-74557delinsAGGC	ENSP00000457914.1:n.46-74560_46-74557delinsAGGC
NM_001220488.1:c.187-74560_187-74557delinsAGGC	NP_001207417.1:n.187-74560_187-74557delinsAGGC
NM_001220489.1:c.46-74560_46-74557delinsAGGC	NP_001207418.1:n.46-74560_46-74557delinsAGGC
NM_001220490.1:c.-508-74560_-508-74557delinsAGGC	NP_001207419.1:n.-508-74560_-508-74557delinsAGGC
NM_001220491.1:c.46-74560_46-74557delinsAGGC	NP_001207420.1:n.46-74560_46-74557delinsAGGC
NM_001220492.1:c.46-74560_46-74557delinsAGGC	NP_001207421.1:n.46-74560_46-74557delinsAGGC
NM_001257.4:c.46-74560_46-74557delinsAGGC	NP_001248.1:n.46-74560_46-74557delinsAGGC
NR_110938.1:n.171+10313_171+10316delinsAGGC
XM_011522805.1:c.187-74560_187-74557delinsAGGC	XP_011521107.1:n.187-74560_187-74557delinsAGGC
XM_017022848.2:c.187-74560_187-74557delinsAGGC	XP_016878337.1:n.187-74560_187-74557delinsAGGC
XM_017022849.2:c.187-74560_187-74557delinsAGGC	XP_016878338.1:n.187-74560_187-74557delinsAGGC
NM_001257.5:c.46-74560_46-74557delinsAGGC MANE Select	NP_001248.1:n.46-74560_46-74557delinsAGGC
NM_001220488.2:c.187-74560_187-74557delinsAGGC	NP_001207417.1:n.187-74560_187-74557delinsAGGC
NM_001220489.2:c.46-74560_46-74557delinsAGGC	NP_001207418.1:n.46-74560_46-74557delinsAGGC
NM_001220490.2:c.-508-74560_-508-74557delinsAGGC	NP_001207419.1:n.-508-74560_-508-74557delinsAGGC
NM_001220491.2:c.46-74560_46-74557delinsAGGC	NP_001207420.1:n.46-74560_46-74557delinsAGGC
NM_001220492.2:c.46-74560_46-74557delinsAGGC	NP_001207421.1:n.46-74560_46-74557delinsAGGC