Canonical Allele Identifier: CA2582342533

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2583671
• ClinVar RCV Id: RCV003334593

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822224_68822234del , CM000678.2:g.68822224_68822234del	GRCh38
NC_000016.9:g.68856127_68856137del , CM000678.1:g.68856127_68856137del	GRCh37
NC_000016.8:g.67413628_67413638del	NCBI36
NG_008021.1:g.89933_89943del , LRG_301:g.89933_89943del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1935_1936+9del
ENST00000261769.9:c.1935_1936+9del
ENST00000422392.6:c.1752_1753+9del
ENST00000562836.5:n.2006_2007+9del
ENST00000566510.5:c.*601_*602+9del
ENST00000566612.5:c.*175_*176+9del
ENST00000611625.4:c.1998_1999+9del
ENST00000612417.4:c.1830+105_1830+115del	ENSP00000478360.1:n.1830+105_1830+115del
ENST00000621016.4:c.1865+70_1865+80del	ENSP00000480664.1:n.1865+70_1865+80del
NM_004360.3:c.1935_1936+9del , LRG_301t1:c.1935_1936+9del
XM_011523488.1:c.1200_1201+9del
XM_011523489.1:c.1200_1201+9del
NM_001317184.1:c.1752_1753+9del
NM_001317185.1:c.387_388+9del
NM_001317186.1:c.-31_-30+9del
NM_004360.4:c.1935_1936+9del
NM_004360.5:c.1935_1936+9del
NM_001317184.2:c.1752_1753+9del
NM_001317185.2:c.387_388+9del
NM_001317186.2:c.-31_-30+9del