Canonical Allele Identifier: CA978522665

Gene: CDH1

Linked Data

• dbSNP Id: rs1758701314
• gnomAD v3: 16-68820058-GT-G
• gnomAD v4: 16-68820058-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68820059del , CM000678.2:g.68820059del	GRCh38
NC_000016.9:g.68853962del , CM000678.1:g.68853962del	GRCh37
NC_000016.8:g.67411463del	NCBI36
NG_008021.1:g.87768del , LRG_301:g.87768del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1711+634del MANE Select	ENSP00000261769.4:n.1711+634del
ENST00000261769.9:c.1711+634del	ENSP00000261769.4:n.1711+634del
ENST00000422392.6:c.1528+634del	ENSP00000414946.2:n.1528+634del
ENST00000562836.5:n.1782+634del
ENST00000566510.5:c.*377+634del	ENSP00000458139.1:n.*377+634del
ENST00000566612.5:c.1566-1942del	ENSP00000454782.1:n.1566-1942del
ENST00000611625.4:c.1774+634del	ENSP00000481063.1:n.1774+634del
ENST00000612417.4:c.1711+634del	ENSP00000478360.1:n.1711+634del
ENST00000621016.4:c.1711+634del	ENSP00000480664.1:n.1711+634del
NM_004360.3:c.1711+634del , LRG_301t1:c.1711+634del	NP_004351.1:n.1711+634del
XM_011523488.1:c.976+634del	XP_011521790.1:n.976+634del
XM_011523489.1:c.976+634del	XP_011521791.1:n.976+634del
NM_001317184.1:c.1528+634del	NP_001304113.1:n.1528+634del
NM_001317185.1:c.163+634del	NP_001304114.1:n.163+634del
NM_001317186.1:c.-254-1942del	NP_001304115.1:n.-254-1942del
NM_004360.4:c.1711+634del	NP_004351.1:n.1711+634del
NM_004360.5:c.1711+634del MANE Select	NP_004351.1:n.1711+634del
NM_001317184.2:c.1528+634del	NP_001304113.1:n.1528+634del
NM_001317185.2:c.163+634del	NP_001304114.1:n.163+634del
NM_001317186.2:c.-254-1942del	NP_001304115.1:n.-254-1942del