Canonical Allele Identifier: CA2580091955
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1759447
ClinVar RCV Id: RCV002393947
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810266_68810344del , CM000678.2:g.68810266_68810344del GRCh38
NC_000016.9:g.68844169_68844247del , CM000678.1:g.68844169_68844247del GRCh37
NC_000016.8:g.67401670_67401748del NCBI36
NG_008021.1:g.77975_78053del , LRG_301:g.77975_78053del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.757_832+3del
ENST00000261769.9:c.757_832+3del
ENST00000422392.6:c.757_832+3del
ENST00000561751.1:c.455-1418_455-1340del
ENST00000562836.5:n.828_903+3del
ENST00000566510.5:c.601_676+3del
ENST00000566612.5:c.757_832+3del
ENST00000611625.4:c.757_832+3del
ENST00000612417.4:c.757_832+3del
ENST00000621016.4:c.757_832+3del
NM_004360.3:c.757_832+3del , LRG_301t1:c.757_832+3del
XM_011523488.1:c.22_97+3del
XM_011523489.1:c.22_97+3del
NM_001317184.1:c.757_832+3del
NM_001317185.1:c.-859_-784+3del
NM_001317186.1:c.-1063_-988+3del
NM_004360.4:c.757_832+3del
NM_004360.5:c.757_832+3del
NM_001317184.2:c.757_832+3del
NM_001317185.2:c.-859_-784+3del
NM_001317186.2:c.-1063_-988+3del
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