Canonical Allele Identifier: CA913188714

Gene: CDH1

Linked Data

• ClinVar Variation Id: 922365
• ClinVar RCV Id: RCV001182402
• dbSNP Id: rs786200947

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737469_68737470delinsTG , CM000678.2:g.68737469_68737470delinsTG	GRCh38
NC_000016.9:g.68771372_68771373delinsTG , CM000678.1:g.68771372_68771373delinsTG	GRCh37
NC_000016.8:g.67328873_67328874delinsTG	NCBI36
NG_008021.1:g.5178_5179delinsTG , LRG_301:g.5178_5179delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.48+6_48+7delinsTG MANE Select	ENSP00000261769.4:n.48+6_48+7delinsTG
ENST00000261769.9:c.48+6_48+7delinsTG	ENSP00000261769.4:n.48+6_48+7delinsTG
ENST00000422392.6:c.48+6_48+7delinsTG	ENSP00000414946.2:n.48+6_48+7delinsTG
ENST00000566510.5:c.48+6_48+7delinsTG	ENSP00000458139.1:n.48+6_48+7delinsTG
ENST00000566612.5:c.48+6_48+7delinsTG	ENSP00000454782.1:n.48+6_48+7delinsTG
ENST00000611625.4:c.48+6_48+7delinsTG	ENSP00000481063.1:n.48+6_48+7delinsTG
ENST00000612417.4:c.48+6_48+7delinsTG	ENSP00000478360.1:n.48+6_48+7delinsTG
ENST00000621016.4:c.48+6_48+7delinsTG	ENSP00000480664.1:n.48+6_48+7delinsTG
NM_004360.3:c.48+6_48+7delinsTG , LRG_301t1:c.48+6_48+7delinsTG	NP_004351.1:n.48+6_48+7delinsTG
NM_001317184.1:c.48+6_48+7delinsTG	NP_001304113.1:n.48+6_48+7delinsTG
NM_001317185.1:c.-1568+6_-1568+7delinsTG	NP_001304114.1:n.-1568+6_-1568+7delinsTG
NM_001317186.1:c.-1772+6_-1772+7delinsTG	NP_001304115.1:n.-1772+6_-1772+7delinsTG
NM_004360.4:c.48+6_48+7delinsTG	NP_004351.1:n.48+6_48+7delinsTG
NM_004360.5:c.48+6_48+7delinsTG MANE Select	NP_004351.1:n.48+6_48+7delinsTG
NM_001317184.2:c.48+6_48+7delinsTG	NP_001304113.1:n.48+6_48+7delinsTG
NM_001317185.2:c.-1568+6_-1568+7delinsTG	NP_001304114.1:n.-1568+6_-1568+7delinsTG
NM_001317186.2:c.-1772+6_-1772+7delinsTG	NP_001304115.1:n.-1772+6_-1772+7delinsTG