Canonical Allele Identifier: CA396465324

Gene: CDH1

Linked Data

• dbSNP Id: rs1961078305
• MyVariant Identifiers: chr16:g.68853291C>A (hg19) ; chr16:g.68819388C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68819388C>A , CM000678.2:g.68819388C>A	GRCh38
NC_000016.9:g.68853291C>A , CM000678.1:g.68853291C>A	GRCh37
NC_000016.8:g.67410792C>A	NCBI36
NG_008021.1:g.87097C>A , LRG_301:g.87097C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1674C>A MANE Select	ENSP00000261769.4:p.Asn558Lys
ENST00000261769.9:c.1674C>A	ENSP00000261769.4:p.Asn558Lys
ENST00000422392.6:c.1491C>A	ENSP00000414946.2:p.Asn497Lys
ENST00000562836.5:n.1745C>A
ENST00000566510.5:c.*340C>A	ENSP00000458139.1:n.*340C>A
ENST00000566612.5:c.1566-2613C>A	ENSP00000454782.1:n.1566-2613C>A
ENST00000611625.4:c.1737C>A	ENSP00000481063.1:p.Asn579Lys
ENST00000612417.4:c.1674C>A	ENSP00000478360.1:p.Asn558Lys
ENST00000621016.4:c.1674C>A	ENSP00000480664.1:p.Asn558Lys
NM_004360.3:c.1674C>A , LRG_301t1:c.1674C>A	NP_004351.1:p.Asn558Lys
XM_011523488.1:c.939C>A	XP_011521790.1:p.Asn313Lys
XM_011523489.1:c.939C>A	XP_011521791.1:p.Asn313Lys
NM_001317184.1:c.1491C>A	NP_001304113.1:p.Asn497Lys
NM_001317185.1:c.126C>A	NP_001304114.1:p.Asn42Lys
NM_001317186.1:c.-254-2613C>A	NP_001304115.1:n.-254-2613C>A
NM_004360.4:c.1674C>A	NP_004351.1:p.Asn558Lys
NM_004360.5:c.1674C>A MANE Select	NP_004351.1:p.Asn558Lys
NM_001317184.2:c.1491C>A	NP_001304113.1:p.Asn497Lys
NM_001317185.2:c.126C>A	NP_001304114.1:p.Asn42Lys
NM_001317186.2:c.-254-2613C>A	NP_001304115.1:n.-254-2613C>A