Canonical Allele Identifier: CA2229982317

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823358_68823378delinsCCTCCCCTGGTCTCATCATTT , CM000678.2:g.68823358_68823378delinsCCTCCCCTGGTCTCATCATTT	GRCh38
NC_000016.9:g.68857261_68857281delinsCCTCCCCTGGTCTCATCATTT , CM000678.1:g.68857261_68857281delinsCCTCCCCTGGTCTCATCATTT	GRCh37
NC_000016.8:g.67414762_67414782delinsCCTCCCCTGGTCTCATCATTT	NCBI36
NG_008021.1:g.91067_91087delinsCCTCCCCTGGTCTCATCATTT , LRG_301:g.91067_91087delinsCCTCCCCTGGTCTCATCATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1937-41_1937-21delinsCCTCCCCTGGTCTCATCATTT MANE Select	ENSP00000261769.4:n.1937-41_1937-21delinsCCTCCCCTGGTCTCATCATT...
ENST00000261769.9:c.1937-41_1937-21delinsCCTCCCCTGGTCTCATCATTT	ENSP00000261769.4:n.1937-41_1937-21delinsCCTCCCCTGGTCTCATCATT...
ENST00000422392.6:c.1754-41_1754-21delinsCCTCCCCTGGTCTCATCATTT	ENSP00000414946.2:n.1754-41_1754-21delinsCCTCCCCTGGTCTCATCATT...
ENST00000562118.1:n.114_134delinsCCTCCCCTGGTCTCATCATTT
ENST00000562836.5:n.2008-41_2008-21delinsCCTCCCCTGGTCTCATCATTT
ENST00000566510.5:c.*603-41_*603-21delinsCCTCCCCTGGTCTCATCATTT	ENSP00000458139.1:n.*603-41_*603-21delinsCCTCCCCTGGTCTCATCATT...
ENST00000566612.5:c.*177-41_*177-21delinsCCTCCCCTGGTCTCATCATTT	ENSP00000454782.1:n.*177-41_*177-21delinsCCTCCCCTGGTCTCATCATT...
ENST00000611625.4:c.2000-41_2000-21delinsCCTCCCCTGGTCTCATCATTT	ENSP00000481063.1:n.2000-41_2000-21delinsCCTCCCCTGGTCTCATCATT...
ENST00000612417.4:c.1830+1239_1830+1259delinsCCTCCCCTGGTCTCATCATTT	ENSP00000478360.1:n.1830+1239_1830+1259delinsCCTCCCCTGGTCTCAT...
ENST00000621016.4:c.1865+1204_1865+1224delinsCCTCCCCTGGTCTCATCATTT	ENSP00000480664.1:n.1865+1204_1865+1224delinsCCTCCCCTGGTCTCAT...
NM_004360.3:c.1937-41_1937-21delinsCCTCCCCTGGTCTCATCATTT , LRG_301t1:c.1937-41_1937-21delinsCCTCCCCTGGTCTCATCATTT	NP_004351.1:n.1937-41_1937-21delinsCCTCCCCTGGTCTCATCATTT
XM_011523488.1:c.1202-41_1202-21delinsCCTCCCCTGGTCTCATCATTT	XP_011521790.1:n.1202-41_1202-21delinsCCTCCCCTGGTCTCATCATTT
XM_011523489.1:c.1202-41_1202-21delinsCCTCCCCTGGTCTCATCATTT	XP_011521791.1:n.1202-41_1202-21delinsCCTCCCCTGGTCTCATCATTT
NM_001317184.1:c.1754-41_1754-21delinsCCTCCCCTGGTCTCATCATTT	NP_001304113.1:n.1754-41_1754-21delinsCCTCCCCTGGTCTCATCATTT
NM_001317185.1:c.389-41_389-21delinsCCTCCCCTGGTCTCATCATTT	NP_001304114.1:n.389-41_389-21delinsCCTCCCCTGGTCTCATCATTT
NM_001317186.1:c.-29-41_-29-21delinsCCTCCCCTGGTCTCATCATTT	NP_001304115.1:n.-29-41_-29-21delinsCCTCCCCTGGTCTCATCATTT
NM_004360.4:c.1937-41_1937-21delinsCCTCCCCTGGTCTCATCATTT	NP_004351.1:n.1937-41_1937-21delinsCCTCCCCTGGTCTCATCATTT
NM_004360.5:c.1937-41_1937-21delinsCCTCCCCTGGTCTCATCATTT MANE Select	NP_004351.1:n.1937-41_1937-21delinsCCTCCCCTGGTCTCATCATTT
NM_001317184.2:c.1754-41_1754-21delinsCCTCCCCTGGTCTCATCATTT	NP_001304113.1:n.1754-41_1754-21delinsCCTCCCCTGGTCTCATCATTT
NM_001317185.2:c.389-41_389-21delinsCCTCCCCTGGTCTCATCATTT	NP_001304114.1:n.389-41_389-21delinsCCTCCCCTGGTCTCATCATTT
NM_001317186.2:c.-29-41_-29-21delinsCCTCCCCTGGTCTCATCATTT	NP_001304115.1:n.-29-41_-29-21delinsCCTCCCCTGGTCTCATCATTT