Canonical Allele Identifier: CA916081842

Gene: CDH1

Linked Data

• ClinVar Variation Id: 845399
• ClinVar RCV Id: RCV001048458

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823632_68830763del , CM000678.2:g.68823632_68830763del	GRCh38
NC_000016.9:g.68857535_68864666del , CM000678.1:g.68857535_68864666del	GRCh37
NC_000016.8:g.67415036_67422167del	NCBI36
NG_008021.1:g.91341_98472del , LRG_301:g.91341_98472del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2164+6_2439+966del
ENST00000261769.9:c.2164+6_2439+966del
ENST00000422392.6:c.1981+6_2256+966del
ENST00000562118.1:n.382+6_657+966del
ENST00000562836.5:n.2235+6_2510+966del
ENST00000566510.5:c.*830+6_*1105+966del
ENST00000566612.5:c.*404+6_*679+966del
ENST00000611625.4:c.2227+6_2502+966del
ENST00000612417.4:c.1830+1513_1854-3428del
ENST00000621016.4:c.1865+1478_1866-3440del	ENSP00000480664.1:n.1865+1478_1866-3440de...
NM_004360.3:c.2164+6_2439+966del , LRG_301t1:c.2164+6_2439+966del
XM_011523488.1:c.1429+6_1704+966del
XM_011523489.1:c.1429+6_1704+966del
NM_001317184.1:c.1981+6_2256+966del
NM_001317185.1:c.616+6_891+966del
NM_001317186.1:c.199+6_474+966del
NM_004360.4:c.2164+6_2439+966del
NM_004360.5:c.2164+6_2439+966del
NM_001317184.2:c.1981+6_2256+966del
NM_001317185.2:c.616+6_891+966del
NM_001317186.2:c.199+6_474+966del