Canonical Allele Identifier: CA913190996

Gene: CDH1

Linked Data

• ClinVar Variation Id: 627901
• ClinVar RCV Id: RCV000772039
• dbSNP Id: rs1567471552

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738414_68738415insGAG , CM000678.2:g.68738414_68738415insGAG	GRCh38
NC_000016.9:g.68772317_68772318insGAG , CM000678.1:g.68772317_68772318insGAG	GRCh37
NC_000016.8:g.67329818_67329819insGAG	NCBI36
NG_008021.1:g.6123_6124insGAG , LRG_301:g.6123_6124insGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.163+3_163+4insGAG MANE Select	ENSP00000261769.4:n.163+3_163+4insGAG
ENST00000261769.9:c.163+3_163+4insGAG	ENSP00000261769.4:n.163+3_163+4insGAG
ENST00000422392.6:c.163+3_163+4insGAG	ENSP00000414946.2:n.163+3_163+4insGAG
ENST00000566510.5:c.163+3_163+4insGAG	ENSP00000458139.1:n.163+3_163+4insGAG
ENST00000566612.5:c.163+3_163+4insGAG	ENSP00000454782.1:n.163+3_163+4insGAG
ENST00000611625.4:c.163+3_163+4insGAG	ENSP00000481063.1:n.163+3_163+4insGAG
ENST00000612417.4:c.163+3_163+4insGAG	ENSP00000478360.1:n.163+3_163+4insGAG
ENST00000621016.4:c.163+3_163+4insGAG	ENSP00000480664.1:n.163+3_163+4insGAG
NM_004360.3:c.163+3_163+4insGAG , LRG_301t1:c.163+3_163+4insGAG	NP_004351.1:n.163+3_163+4insGAG
NM_001317184.1:c.163+3_163+4insGAG	NP_001304113.1:n.163+3_163+4insGAG
NM_001317185.1:c.-1453+3_-1453+4insGAG	NP_001304114.1:n.-1453+3_-1453+4insGAG
NM_001317186.1:c.-1657+3_-1657+4insGAG	NP_001304115.1:n.-1657+3_-1657+4insGAG
NM_004360.4:c.163+3_163+4insGAG	NP_004351.1:n.163+3_163+4insGAG
NM_004360.5:c.163+3_163+4insGAG MANE Select	NP_004351.1:n.163+3_163+4insGAG
NM_001317184.2:c.163+3_163+4insGAG	NP_001304113.1:n.163+3_163+4insGAG
NM_001317185.2:c.-1453+3_-1453+4insGAG	NP_001304114.1:n.-1453+3_-1453+4insGAG
NM_001317186.2:c.-1657+3_-1657+4insGAG	NP_001304115.1:n.-1657+3_-1657+4insGAG