Canonical Allele Identifier: CA298961

Gene: CDH1

Linked Data

• ClinVar Variation Id: 182388
• ClinVar RCV Id: RCV000160380
• dbSNP Id: rs730881659
• gnomAD v2: 16-68771297-C-A
• gnomAD v4: 16-68737394-C-A
• MyVariant Identifiers: chr16:g.68771297C>A (hg19) ; chr16:g.68737394C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737394C>A , CM000678.2:g.68737394C>A	GRCh38
NC_000016.9:g.68771297C>A , CM000678.1:g.68771297C>A	GRCh37
NC_000016.8:g.67328798C>A	NCBI36
NG_008021.1:g.5103C>A , LRG_301:g.5103C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.-22C>A MANE Select	ENSP00000261769.4:n.-22C>A
ENST00000261769.9:c.-22C>A	ENSP00000261769.4:n.-22C>A
ENST00000422392.6:c.-22C>A	ENSP00000414946.2:n.-22C>A
ENST00000566510.5:c.-22C>A	ENSP00000458139.1:n.-22C>A
ENST00000566612.5:c.-22C>A	ENSP00000454782.1:n.-22C>A
ENST00000611625.4:c.-22C>A	ENSP00000481063.1:n.-22C>A
ENST00000612417.4:c.-22C>A	ENSP00000478360.1:n.-22C>A
ENST00000621016.4:c.-22C>A	ENSP00000480664.1:n.-22C>A
NM_004360.3:c.-22C>A , LRG_301t1:c.-22C>A	NP_004351.1:n.-22C>A
NM_001317184.1:c.-22C>A	NP_001304113.1:n.-22C>A
NM_001317185.1:c.-1637C>A	NP_001304114.1:n.-1637C>A
NM_001317186.1:c.-1841C>A	NP_001304115.1:n.-1841C>A
NM_004360.4:c.-22C>A	NP_004351.1:n.-22C>A
NM_004360.5:c.-22C>A MANE Select	NP_004351.1:n.-22C>A
NM_001317184.2:c.-22C>A	NP_001304113.1:n.-22C>A
NM_001317185.2:c.-1637C>A	NP_001304114.1:n.-1637C>A
NM_001317186.2:c.-1841C>A	NP_001304115.1:n.-1841C>A