Canonical Allele Identifier: CA396471212

Gene: CDH1

Linked Data

• dbSNP Id: rs876660704
• MyVariant Identifiers: chr16:g.68863662C>A (hg19) ; chr16:g.68829759C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829759C>A , CM000678.2:g.68829759C>A	GRCh38
NC_000016.9:g.68863662C>A , CM000678.1:g.68863662C>A	GRCh37
NC_000016.8:g.67421163C>A	NCBI36
NG_008021.1:g.97468C>A , LRG_301:g.97468C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2401C>A MANE Select	ENSP00000261769.4:p.Pro801Thr
ENST00000261769.9:c.2401C>A	ENSP00000261769.4:p.Pro801Thr
ENST00000422392.6:c.2218C>A	ENSP00000414946.2:p.Pro740Thr
ENST00000562118.1:n.619C>A
ENST00000562836.5:n.2472C>A
ENST00000566510.5:c.*1067C>A	ENSP00000458139.1:n.*1067C>A
ENST00000566612.5:c.*641C>A	ENSP00000454782.1:n.*641C>A
ENST00000611625.4:c.2464C>A	ENSP00000481063.1:p.Pro822Thr
ENST00000612417.4:c.1853+3205C>A	ENSP00000478360.1:n.1853+3205C>A
ENST00000621016.4:c.1866-4444C>A	ENSP00000480664.1:n.1866-4444C>A
NM_004360.3:c.2401C>A , LRG_301t1:c.2401C>A	NP_004351.1:p.Pro801Thr
XM_011523488.1:c.1666C>A	XP_011521790.1:p.Pro556Thr
XM_011523489.1:c.1666C>A	XP_011521791.1:p.Pro556Thr
NM_001317184.1:c.2218C>A	NP_001304113.1:p.Pro740Thr
NM_001317185.1:c.853C>A	NP_001304114.1:p.Pro285Thr
NM_001317186.1:c.436C>A	NP_001304115.1:p.Pro146Thr
NM_004360.4:c.2401C>A	NP_004351.1:p.Pro801Thr
NM_004360.5:c.2401C>A MANE Select	NP_004351.1:p.Pro801Thr
NM_001317184.2:c.2218C>A	NP_001304113.1:p.Pro740Thr
NM_001317185.2:c.853C>A	NP_001304114.1:p.Pro285Thr
NM_001317186.2:c.436C>A	NP_001304115.1:p.Pro146Thr