Canonical Allele Identifier: CA396452334

Gene: CDH1

Linked Data

• ClinVar Variation Id: 819725
• ClinVar RCV Id: RCV001012528 ; RCV003624439
• dbSNP Id: rs1597838766
• MyVariant Identifiers: chr16:g.68772314G>A (hg19) ; chr16:g.68738411G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738411G>A , CM000678.2:g.68738411G>A	GRCh38
NC_000016.9:g.68772314G>A , CM000678.1:g.68772314G>A	GRCh37
NC_000016.8:g.67329815G>A	NCBI36
NG_008021.1:g.6120G>A , LRG_301:g.6120G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.163G>A MANE Select	ENSP00000261769.4:p.Val55Met
ENST00000261769.9:c.163G>A	ENSP00000261769.4:p.Val55Met
ENST00000422392.6:c.163G>A	ENSP00000414946.2:p.Val55Met
ENST00000566510.5:c.163G>A	ENSP00000458139.1:p.Val55Met
ENST00000566612.5:c.163G>A	ENSP00000454782.1:p.Val55Met
ENST00000611625.4:c.163G>A	ENSP00000481063.1:p.Val55Met
ENST00000612417.4:c.163G>A	ENSP00000478360.1:p.Val55Met
ENST00000621016.4:c.163G>A	ENSP00000480664.1:p.Val55Met
NM_004360.3:c.163G>A , LRG_301t1:c.163G>A	NP_004351.1:p.Val55Met
NM_001317184.1:c.163G>A	NP_001304113.1:p.Val55Met
NM_001317185.1:c.-1453G>A	NP_001304114.1:n.-1453G>A
NM_001317186.1:c.-1657G>A	NP_001304115.1:n.-1657G>A
NM_004360.4:c.163G>A	NP_004351.1:p.Val55Met
NM_004360.5:c.163G>A MANE Select	NP_004351.1:p.Val55Met
NM_001317184.2:c.163G>A	NP_001304113.1:p.Val55Met
NM_001317185.2:c.-1453G>A	NP_001304114.1:n.-1453G>A
NM_001317186.2:c.-1657G>A	NP_001304115.1:n.-1657G>A