Canonical Allele Identifier: CA396462852

Gene: CDH1

Linked Data

• dbSNP Id: rs2152134801
• MyVariant Identifiers: chr16:g.68849481T>A (hg19) ; chr16:g.68815578T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815578T>A , CM000678.2:g.68815578T>A	GRCh38
NC_000016.9:g.68849481T>A , CM000678.1:g.68849481T>A	GRCh37
NC_000016.8:g.67406982T>A	NCBI36
NG_008021.1:g.83287T>A , LRG_301:g.83287T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1384T>A MANE Select	ENSP00000261769.4:p.Phe462Ile
ENST00000261769.9:c.1384T>A	ENSP00000261769.4:p.Phe462Ile
ENST00000422392.6:c.1201T>A	ENSP00000414946.2:p.Phe401Ile
ENST00000562836.5:n.1455T>A
ENST00000566510.5:c.*50T>A	ENSP00000458139.1:n.*50T>A
ENST00000566612.5:c.1384T>A	ENSP00000454782.1:p.Phe462Ile
ENST00000611625.4:c.1447T>A	ENSP00000481063.1:p.Phe483Ile
ENST00000612417.4:c.1384T>A	ENSP00000478360.1:p.Phe462Ile
ENST00000621016.4:c.1384T>A	ENSP00000480664.1:p.Phe462Ile
NM_004360.3:c.1384T>A , LRG_301t1:c.1384T>A	NP_004351.1:p.Phe462Ile
XM_011523488.1:c.649T>A	XP_011521790.1:p.Phe217Ile
XM_011523489.1:c.649T>A	XP_011521791.1:p.Phe217Ile
NM_001317184.1:c.1201T>A	NP_001304113.1:p.Phe401Ile
NM_001317185.1:c.-165T>A	NP_001304114.1:n.-165T>A
NM_001317186.1:c.-436T>A	NP_001304115.1:n.-436T>A
NM_004360.4:c.1384T>A	NP_004351.1:p.Phe462Ile
NM_004360.5:c.1384T>A MANE Select	NP_004351.1:p.Phe462Ile
NM_001317184.2:c.1201T>A	NP_001304113.1:p.Phe401Ile
NM_001317185.2:c.-165T>A	NP_001304114.1:n.-165T>A
NM_001317186.2:c.-436T>A	NP_001304115.1:n.-436T>A