Canonical Allele Identifier: CA2229977943

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68819317_68819318delinsAT , CM000678.2:g.68819317_68819318delinsAT	GRCh38
NC_000016.9:g.68853220_68853221delinsAT , CM000678.1:g.68853220_68853221delinsAT	GRCh37
NC_000016.8:g.67410721_67410722delinsAT	NCBI36
NG_008021.1:g.87026_87027delinsAT , LRG_301:g.87026_87027delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1603_1604delinsAT MANE Select	ENSP00000261769.4:p.Ile535=
ENST00000261769.9:c.1603_1604delinsAT	ENSP00000261769.4:p.Ile535=
ENST00000422392.6:c.1420_1421delinsAT	ENSP00000414946.2:p.Ile474=
ENST00000562836.5:n.1674_1675delinsAT
ENST00000566510.5:c.*269_*270delinsAT	ENSP00000458139.1:n.*269_*270delinsAT
ENST00000566612.5:c.1566-2684_1566-2683delinsAT	ENSP00000454782.1:n.1566-2684_1566-2683de...
ENST00000611625.4:c.1666_1667delinsAT	ENSP00000481063.1:p.Ile556=
ENST00000612417.4:c.1603_1604delinsAT	ENSP00000478360.1:p.Ile535=
ENST00000621016.4:c.1603_1604delinsAT	ENSP00000480664.1:p.Ile535=
NM_004360.3:c.1603_1604delinsAT , LRG_301t1:c.1603_1604delinsAT	NP_004351.1:p.Ile535=
XM_011523488.1:c.868_869delinsAT	XP_011521790.1:p.Ile290=
XM_011523489.1:c.868_869delinsAT	XP_011521791.1:p.Ile290=
NM_001317184.1:c.1420_1421delinsAT	NP_001304113.1:p.Ile474=
NM_001317185.1:c.55_56delinsAT	NP_001304114.1:p.Ile19=
NM_001317186.1:c.-254-2684_-254-2683delinsAT	NP_001304115.1:n.-254-2684_-254-2683delin...
NM_004360.4:c.1603_1604delinsAT	NP_004351.1:p.Ile535=
NM_004360.5:c.1603_1604delinsAT MANE Select	NP_004351.1:p.Ile535=
NM_001317184.2:c.1420_1421delinsAT	NP_001304113.1:p.Ile474=
NM_001317185.2:c.55_56delinsAT	NP_001304114.1:p.Ile19=
NM_001317186.2:c.-254-2684_-254-2683delinsAT	NP_001304115.1:n.-254-2684_-254-2683delin...