Canonical Allele Identifier: CA2229988890
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68827764_68827779delinsCCATGTCTCTTCCCCT , CM000678.2:g.68827764_68827779delinsCCATGTCTCTTCCCCT GRCh38
NC_000016.9:g.68861667_68861682delinsCCATGTCTCTTCCCCT , CM000678.1:g.68861667_68861682delinsCCATGTCTCTTCCCCT GRCh37
NC_000016.8:g.67419168_67419183delinsCCATGTCTCTTCCCCT NCBI36
NG_008021.1:g.95473_95488delinsCCATGTCTCTTCCCCT , LRG_301:g.95473_95488delinsCCATGTCTCTTCCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2165-410_2165-395delinsCCATGTCTCTTCCCCT MANE Select ENSP00000261769.4:n.2165-410_2165-395delinsCCATGTCTCTTCCCCT
ENST00000261769.9:c.2165-410_2165-395delinsCCATGTCTCTTCCCCT ENSP00000261769.4:n.2165-410_2165-395delinsCCATGTCTCTTCCCCT
ENST00000422392.6:c.1982-410_1982-395delinsCCATGTCTCTTCCCCT ENSP00000414946.2:n.1982-410_1982-395delinsCCATGTCTCTTCCCCT
ENST00000562118.1:n.383-410_383-395delinsCCATGTCTCTTCCCCT
ENST00000562836.5:n.2236-410_2236-395delinsCCATGTCTCTTCCCCT
ENST00000566510.5:c.*831-410_*831-395delinsCCATGTCTCTTCCCCT ENSP00000458139.1:n.*831-410_*831-395delinsCCATGTCTCTTCCCCT
ENST00000566612.5:c.*405-410_*405-395delinsCCATGTCTCTTCCCCT ENSP00000454782.1:n.*405-410_*405-395delinsCCATGTCTCTTCCCCT
ENST00000611625.4:c.2228-410_2228-395delinsCCATGTCTCTTCCCCT ENSP00000481063.1:n.2228-410_2228-395delinsCCATGTCTCTTCCCCT
ENST00000612417.4:c.1853+1210_1853+1225delinsCCATGTCTCTTCCCCT ENSP00000478360.1:n.1853+1210_1853+1225delinsCCATGTCTCTTCCCCT...
ENST00000621016.4:c.1865+5610_1865+5625delinsCCATGTCTCTTCCCCT ENSP00000480664.1:n.1865+5610_1865+5625delinsCCATGTCTCTTCCCCT...
NM_004360.3:c.2165-410_2165-395delinsCCATGTCTCTTCCCCT , LRG_301t1:c.2165-410_2165-395delinsCCATGTCTCTTCCCCT NP_004351.1:n.2165-410_2165-395delinsCCATGTCTCTTCCCCT
XM_011523488.1:c.1430-410_1430-395delinsCCATGTCTCTTCCCCT XP_011521790.1:n.1430-410_1430-395delinsCCATGTCTCTTCCCCT
XM_011523489.1:c.1430-410_1430-395delinsCCATGTCTCTTCCCCT XP_011521791.1:n.1430-410_1430-395delinsCCATGTCTCTTCCCCT
NM_001317184.1:c.1982-410_1982-395delinsCCATGTCTCTTCCCCT NP_001304113.1:n.1982-410_1982-395delinsCCATGTCTCTTCCCCT
NM_001317185.1:c.617-410_617-395delinsCCATGTCTCTTCCCCT NP_001304114.1:n.617-410_617-395delinsCCATGTCTCTTCCCCT
NM_001317186.1:c.200-410_200-395delinsCCATGTCTCTTCCCCT NP_001304115.1:n.200-410_200-395delinsCCATGTCTCTTCCCCT
NM_004360.4:c.2165-410_2165-395delinsCCATGTCTCTTCCCCT NP_004351.1:n.2165-410_2165-395delinsCCATGTCTCTTCCCCT
NM_004360.5:c.2165-410_2165-395delinsCCATGTCTCTTCCCCT MANE Select NP_004351.1:n.2165-410_2165-395delinsCCATGTCTCTTCCCCT
NM_001317184.2:c.1982-410_1982-395delinsCCATGTCTCTTCCCCT NP_001304113.1:n.1982-410_1982-395delinsCCATGTCTCTTCCCCT
NM_001317185.2:c.617-410_617-395delinsCCATGTCTCTTCCCCT NP_001304114.1:n.617-410_617-395delinsCCATGTCTCTTCCCCT
NM_001317186.2:c.200-410_200-395delinsCCATGTCTCTTCCCCT NP_001304115.1:n.200-410_200-395delinsCCATGTCTCTTCCCCT