Canonical Allele Identifier: CA2807473123

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810078_68810080del , CM000678.2:g.68810078_68810080del	GRCh38
NC_000016.9:g.68843981_68843983del , CM000678.1:g.68843981_68843983del	GRCh37
NC_000016.8:g.67401482_67401484del	NCBI36
NG_008021.1:g.77787_77789del , LRG_301:g.77787_77789del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.688-119_688-117del MANE Select	ENSP00000261769.4:n.688-119_688-117del
ENST00000261769.9:c.688-119_688-117del	ENSP00000261769.4:n.688-119_688-117del
ENST00000422392.6:c.688-119_688-117del	ENSP00000414946.2:n.688-119_688-117del
ENST00000561751.1:c.454+1230_454+1232del
ENST00000562836.5:n.759-119_759-117del
ENST00000566510.5:c.532-119_532-117del	ENSP00000458139.1:n.532-119_532-117del
ENST00000566612.5:c.688-119_688-117del	ENSP00000454782.1:n.688-119_688-117del
ENST00000611625.4:c.688-119_688-117del	ENSP00000481063.1:n.688-119_688-117del
ENST00000612417.4:c.688-119_688-117del	ENSP00000478360.1:n.688-119_688-117del
ENST00000621016.4:c.688-119_688-117del	ENSP00000480664.1:n.688-119_688-117del
NM_004360.3:c.688-119_688-117del , LRG_301t1:c.688-119_688-117del	NP_004351.1:n.688-119_688-117del
XM_011523488.1:c.-48-119_-48-117del	XP_011521790.1:n.-48-119_-48-117del
XM_011523489.1:c.-48-119_-48-117del	XP_011521791.1:n.-48-119_-48-117del
NM_001317184.1:c.688-119_688-117del	NP_001304113.1:n.688-119_688-117del
NM_001317185.1:c.-928-119_-928-117del	NP_001304114.1:n.-928-119_-928-117del
NM_001317186.1:c.-1132-119_-1132-117del	NP_001304115.1:n.-1132-119_-1132-117del
NM_004360.4:c.688-119_688-117del	NP_004351.1:n.688-119_688-117del
NM_004360.5:c.688-119_688-117del MANE Select	NP_004351.1:n.688-119_688-117del
NM_001317184.2:c.688-119_688-117del	NP_001304113.1:n.688-119_688-117del
NM_001317185.2:c.-928-119_-928-117del	NP_001304114.1:n.-928-119_-928-117del
NM_001317186.2:c.-1132-119_-1132-117del	NP_001304115.1:n.-1132-119_-1132-117del