Canonical Allele Identifier: CA2582342548

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2583488
• ClinVar RCV Id: RCV003337159

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801649_68801794del , CM000678.2:g.68801649_68801794del	GRCh38
NC_000016.9:g.68835552_68835697del , CM000678.1:g.68835552_68835697del	GRCh37
NC_000016.8:g.67393053_67393198del	NCBI36
NG_008021.1:g.69358_69503del , LRG_301:g.69358_69503del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.164-21_288del
ENST00000261769.9:c.164-21_288del
ENST00000422392.6:c.164-21_288del
ENST00000562836.5:n.235-21_359del
ENST00000564676.5:n.446-21_570del
ENST00000564745.1:n.159-21_283del
ENST00000566510.5:c.164-21_288del
ENST00000566612.5:c.164-21_288del
ENST00000611625.4:c.164-21_288del
ENST00000612417.4:c.164-21_288del
ENST00000621016.4:c.164-21_288del
NM_004360.3:c.164-21_288del , LRG_301t1:c.164-21_288del
XM_011523488.1:c.-572-21_-448del
XM_011523489.1:c.-572-21_-448del
NM_001317184.1:c.164-21_288del
NM_001317185.1:c.-1452-21_-1328del
NM_001317186.1:c.-1656-21_-1532del
NM_004360.4:c.164-21_288del
NM_004360.5:c.164-21_288del
NM_001317184.2:c.164-21_288del
NM_001317185.2:c.-1452-21_-1328del
NM_001317186.2:c.-1656-21_-1532del