Canonical Allele Identifier: CA2582342590

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2583577
• ClinVar RCV Id: RCV003334499

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815506_68815525dup , CM000678.2:g.68815506_68815525dup	GRCh38
NC_000016.9:g.68849409_68849428dup , CM000678.1:g.68849409_68849428dup	GRCh37
NC_000016.8:g.67406910_67406929dup	NCBI36
NG_008021.1:g.83215_83234dup , LRG_301:g.83215_83234dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1321-9_1331dup
ENST00000261769.9:c.1321-9_1331dup
ENST00000422392.6:c.1138-9_1148dup
ENST00000562836.5:n.1392-9_1402dup
ENST00000566510.5:c.1232-9_1242dup
ENST00000566612.5:c.1321-9_1331dup
ENST00000611625.4:c.1384-9_1394dup
ENST00000612417.4:c.1321-9_1331dup
ENST00000621016.4:c.1321-9_1331dup
NM_004360.3:c.1321-9_1331dup , LRG_301t1:c.1321-9_1331dup
XM_011523488.1:c.586-9_596dup
XM_011523489.1:c.586-9_596dup
NM_001317184.1:c.1138-9_1148dup
NM_001317185.1:c.-228-9_-218dup
NM_001317186.1:c.-499-9_-489dup
NM_004360.4:c.1321-9_1331dup
NM_004360.5:c.1321-9_1331dup
NM_001317184.2:c.1138-9_1148dup
NM_001317185.2:c.-228-9_-218dup
NM_001317186.2:c.-499-9_-489dup