Canonical Allele Identifier: CA1139664754

Gene: CDH1

Linked Data

• ClinVar Variation Id: 933763
• ClinVar RCV Id: RCV001202040
• dbSNP Id: rs1960785868

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810321_68811120del , CM000678.2:g.68810321_68811120del	GRCh38
NC_000016.9:g.68844224_68845023del , CM000678.1:g.68844224_68845023del	GRCh37
NC_000016.8:g.67401725_67402524del	NCBI36
NG_008021.1:g.78030_78829del , LRG_301:g.78030_78829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.812_833-564del
ENST00000261769.9:c.812_833-564del
ENST00000422392.6:c.812_833-564del
ENST00000561751.1:c.455-1363_455-564del
ENST00000562836.5:n.883_904-564del
ENST00000566510.5:c.656_677-564del
ENST00000566612.5:c.812_833-564del
ENST00000611625.4:c.812_833-564del
ENST00000612417.4:c.812_833-564del
ENST00000621016.4:c.812_833-564del
NM_004360.3:c.812_833-564del , LRG_301t1:c.812_833-564del
XM_011523488.1:c.77_98-564del
XM_011523489.1:c.77_98-564del
NM_001317184.1:c.812_833-564del
NM_001317185.1:c.-804_-783-564del
NM_001317186.1:c.-1008_-987-564del
NM_004360.4:c.812_833-564del
NM_004360.5:c.812_833-564del
NM_001317184.2:c.812_833-564del
NM_001317185.2:c.-804_-783-564del
NM_001317186.2:c.-1008_-987-564del