Canonical Allele Identifier: CA2633932378

Gene: CDH1

Linked Data

• gnomAD v4: 16-68823253-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823253_68823254insTT , CM000678.2:g.68823253_68823254insTT	GRCh38
NC_000016.9:g.68857156_68857157insTT , CM000678.1:g.68857156_68857157insTT	GRCh37
NC_000016.8:g.67414657_67414658insTT	NCBI36
NG_008021.1:g.90962_90963insTT , LRG_301:g.90962_90963insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1937-146_1937-145insTT MANE Select	ENSP00000261769.4:n.1937-146_1937-145insTT
ENST00000261769.9:c.1937-146_1937-145insTT	ENSP00000261769.4:n.1937-146_1937-145insTT
ENST00000422392.6:c.1754-146_1754-145insTT	ENSP00000414946.2:n.1754-146_1754-145insTT
ENST00000562118.1:n.9_10insTT
ENST00000562836.5:n.2008-146_2008-145insTT
ENST00000566510.5:c.*603-146_*603-145insTT	ENSP00000458139.1:n.*603-146_*603-145insTT
ENST00000566612.5:c.*177-146_*177-145insTT	ENSP00000454782.1:n.*177-146_*177-145insTT
ENST00000611625.4:c.2000-146_2000-145insTT	ENSP00000481063.1:n.2000-146_2000-145insTT
ENST00000612417.4:c.1830+1134_1830+1135insTT	ENSP00000478360.1:n.1830+1134_1830+1135insTT
ENST00000621016.4:c.1865+1099_1865+1100insTT	ENSP00000480664.1:n.1865+1099_1865+1100insTT
NM_004360.3:c.1937-146_1937-145insTT , LRG_301t1:c.1937-146_1937-145insTT	NP_004351.1:n.1937-146_1937-145insTT
XM_011523488.1:c.1202-146_1202-145insTT	XP_011521790.1:n.1202-146_1202-145insTT
XM_011523489.1:c.1202-146_1202-145insTT	XP_011521791.1:n.1202-146_1202-145insTT
NM_001317184.1:c.1754-146_1754-145insTT	NP_001304113.1:n.1754-146_1754-145insTT
NM_001317185.1:c.389-146_389-145insTT	NP_001304114.1:n.389-146_389-145insTT
NM_001317186.1:c.-29-146_-29-145insTT	NP_001304115.1:n.-29-146_-29-145insTT
NM_004360.4:c.1937-146_1937-145insTT	NP_004351.1:n.1937-146_1937-145insTT
NM_004360.5:c.1937-146_1937-145insTT MANE Select	NP_004351.1:n.1937-146_1937-145insTT
NM_001317184.2:c.1754-146_1754-145insTT	NP_001304113.1:n.1754-146_1754-145insTT
NM_001317185.2:c.389-146_389-145insTT	NP_001304114.1:n.389-146_389-145insTT
NM_001317186.2:c.-29-146_-29-145insTT	NP_001304115.1:n.-29-146_-29-145insTT