Canonical Allele Identifier: CA658798617

Gene: CDH1

Linked Data

• ClinVar Variation Id: 532440
• ClinVar RCV Id: RCV000639207
• dbSNP Id: rs1555509779
• MyVariant Identifiers: chr16:g.68772297_68772314del (hg19) ; chr16:g.68738394_68738411del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738395_68738412del , CM000678.2:g.68738395_68738412del	GRCh38
NC_000016.9:g.68772298_68772315del , CM000678.1:g.68772298_68772315del	GRCh37
NC_000016.8:g.67329799_67329816del	NCBI36
NG_008021.1:g.6104_6121del , LRG_301:g.6104_6121del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.147_163+1del
ENST00000261769.9:c.147_163+1del
ENST00000422392.6:c.147_163+1del
ENST00000566510.5:c.147_163+1del
ENST00000566612.5:c.147_163+1del
ENST00000611625.4:c.147_163+1del
ENST00000612417.4:c.147_163+1del
ENST00000621016.4:c.147_163+1del
NM_004360.3:c.147_163+1del , LRG_301t1:c.147_163+1del
NM_001317184.1:c.147_163+1del
NM_001317185.1:c.-1469_-1453+1del
NM_001317186.1:c.-1673_-1657+1del
NM_004360.4:c.147_163+1del
NM_004360.5:c.147_163+1del
NM_001317184.2:c.147_163+1del
NM_001317185.2:c.-1469_-1453+1del
NM_001317186.2:c.-1673_-1657+1del