Canonical Allele Identifier: CA16615356

Gene: CDH1

Linked Data

• ClinVar Variation Id: 406636
• ClinVar RCV Id: RCV000473205
• dbSNP Id: rs1060501227
• MyVariant Identifiers: chr16:g.68835575A>G (hg19) ; chr16:g.68801672A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801672A>G , CM000678.2:g.68801672A>G	GRCh38
NC_000016.9:g.68835575A>G , CM000678.1:g.68835575A>G	GRCh37
NC_000016.8:g.67393076A>G	NCBI36
NG_008021.1:g.69381A>G , LRG_301:g.69381A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.166A>G MANE Select	ENSP00000261769.4:p.Asn56Asp
ENST00000261769.9:c.166A>G	ENSP00000261769.4:p.Asn56Asp
ENST00000422392.6:c.166A>G	ENSP00000414946.2:p.Asn56Asp
ENST00000562836.5:n.237A>G
ENST00000564676.5:n.448A>G
ENST00000564745.1:n.161A>G
ENST00000566510.5:c.166A>G	ENSP00000458139.1:p.Asn56Asp
ENST00000566612.5:c.166A>G	ENSP00000454782.1:p.Asn56Asp
ENST00000611625.4:c.166A>G	ENSP00000481063.1:p.Asn56Asp
ENST00000612417.4:c.166A>G	ENSP00000478360.1:p.Asn56Asp
ENST00000621016.4:c.166A>G	ENSP00000480664.1:p.Asn56Asp
NM_004360.3:c.166A>G , LRG_301t1:c.166A>G	NP_004351.1:p.Asn56Asp
XM_011523488.1:c.-570A>G	XP_011521790.1:n.-570A>G
XM_011523489.1:c.-570A>G	XP_011521791.1:n.-570A>G
NM_001317184.1:c.166A>G	NP_001304113.1:p.Asn56Asp
NM_001317185.1:c.-1450A>G	NP_001304114.1:n.-1450A>G
NM_001317186.1:c.-1654A>G	NP_001304115.1:n.-1654A>G
NM_004360.4:c.166A>G	NP_004351.1:p.Asn56Asp
NM_004360.5:c.166A>G MANE Select	NP_004351.1:p.Asn56Asp
NM_001317184.2:c.166A>G	NP_001304113.1:p.Asn56Asp
NM_001317185.2:c.-1450A>G	NP_001304114.1:n.-1450A>G
NM_001317186.2:c.-1654A>G	NP_001304115.1:n.-1654A>G