Canonical Allele Identifier: CA2633932376

Gene: CDH1

Linked Data

• gnomAD v4: 16-68823252-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823252_68823253insG , CM000678.2:g.68823252_68823253insG	GRCh38
NC_000016.9:g.68857155_68857156insG , CM000678.1:g.68857155_68857156insG	GRCh37
NC_000016.8:g.67414656_67414657insG	NCBI36
NG_008021.1:g.90961_90962insG , LRG_301:g.90961_90962insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1937-147_1937-146insG MANE Select	ENSP00000261769.4:n.1937-147_1937-146insG
ENST00000261769.9:c.1937-147_1937-146insG	ENSP00000261769.4:n.1937-147_1937-146insG
ENST00000422392.6:c.1754-147_1754-146insG	ENSP00000414946.2:n.1754-147_1754-146insG
ENST00000562118.1:n.8_9insG
ENST00000562836.5:n.2008-147_2008-146insG
ENST00000566510.5:c.*603-147_*603-146insG	ENSP00000458139.1:n.*603-147_*603-146insG
ENST00000566612.5:c.*177-147_*177-146insG	ENSP00000454782.1:n.*177-147_*177-146insG
ENST00000611625.4:c.2000-147_2000-146insG	ENSP00000481063.1:n.2000-147_2000-146insG
ENST00000612417.4:c.1830+1133_1830+1134insG	ENSP00000478360.1:n.1830+1133_1830+1134insG
ENST00000621016.4:c.1865+1098_1865+1099insG	ENSP00000480664.1:n.1865+1098_1865+1099insG
NM_004360.3:c.1937-147_1937-146insG , LRG_301t1:c.1937-147_1937-146insG	NP_004351.1:n.1937-147_1937-146insG
XM_011523488.1:c.1202-147_1202-146insG	XP_011521790.1:n.1202-147_1202-146insG
XM_011523489.1:c.1202-147_1202-146insG	XP_011521791.1:n.1202-147_1202-146insG
NM_001317184.1:c.1754-147_1754-146insG	NP_001304113.1:n.1754-147_1754-146insG
NM_001317185.1:c.389-147_389-146insG	NP_001304114.1:n.389-147_389-146insG
NM_001317186.1:c.-29-147_-29-146insG	NP_001304115.1:n.-29-147_-29-146insG
NM_004360.4:c.1937-147_1937-146insG	NP_004351.1:n.1937-147_1937-146insG
NM_004360.5:c.1937-147_1937-146insG MANE Select	NP_004351.1:n.1937-147_1937-146insG
NM_001317184.2:c.1754-147_1754-146insG	NP_001304113.1:n.1754-147_1754-146insG
NM_001317185.2:c.389-147_389-146insG	NP_001304114.1:n.389-147_389-146insG
NM_001317186.2:c.-29-147_-29-146insG	NP_001304115.1:n.-29-147_-29-146insG