Canonical Allele Identifier: CA913190507

Gene: CDH1

Linked Data

• ClinVar Variation Id: 619669
• ClinVar RCV Id: RCV000759021

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833290_68833499del , CM000678.2:g.68833290_68833499del	GRCh38
NC_000016.9:g.68867193_68867402del , CM000678.1:g.68867193_68867402del	GRCh37
NC_000016.8:g.67424694_67424903del	NCBI36
NG_008021.1:g.100999_101208del , LRG_301:g.100999_101208del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2440_2649del
ENST00000261769.9:c.2440_2649del
ENST00000422392.6:c.2257_2466del
ENST00000562118.1:n.658_867del
ENST00000562836.5:n.2511_2720del
ENST00000566510.5:c.*1106_*1315del
ENST00000566612.5:c.*680_*889del
ENST00000611625.4:c.2503_2712del
ENST00000612417.4:c.1854-901_1854-692del	ENSP00000478360.1:n.1854-901_1854-692del
ENST00000621016.4:c.1866-913_1866-704del	ENSP00000480664.1:n.1866-913_1866-704del
NM_004360.3:c.2440_2649del , LRG_301t1:c.2440_2649del
XM_011523488.1:c.1705_1914del
XM_011523489.1:c.1705_1914del
NM_001317184.1:c.2257_2466del
NM_001317185.1:c.892_1101del
NM_001317186.1:c.475_684del
NM_004360.4:c.2440_2649del
NM_004360.5:c.2440_2649del
NM_001317184.2:c.2257_2466del
NM_001317185.2:c.892_1101del
NM_001317186.2:c.475_684del