Canonical Allele Identifier: CA396467080

Gene: CDH1

Linked Data

• dbSNP Id: rs1961165900
• MyVariant Identifiers: chr16:g.68856062T>A (hg19) ; chr16:g.68822159T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822159T>A , CM000678.2:g.68822159T>A	GRCh38
NC_000016.9:g.68856062T>A , CM000678.1:g.68856062T>A	GRCh37
NC_000016.8:g.67413563T>A	NCBI36
NG_008021.1:g.89868T>A , LRG_301:g.89868T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1870T>A MANE Select	ENSP00000261769.4:p.Ser624Thr
ENST00000261769.9:c.1870T>A	ENSP00000261769.4:p.Ser624Thr
ENST00000422392.6:c.1687T>A	ENSP00000414946.2:p.Ser563Thr
ENST00000562836.5:n.1941T>A
ENST00000566510.5:c.*536T>A	ENSP00000458139.1:n.*536T>A
ENST00000566612.5:c.*110T>A	ENSP00000454782.1:n.*110T>A
ENST00000611625.4:c.1933T>A	ENSP00000481063.1:p.Ser645Thr
ENST00000612417.4:c.1830+40T>A	ENSP00000478360.1:n.1830+40T>A
ENST00000621016.4:c.1865+5T>A	ENSP00000480664.1:n.1865+5T>A
NM_004360.3:c.1870T>A , LRG_301t1:c.1870T>A	NP_004351.1:p.Ser624Thr
XM_011523488.1:c.1135T>A	XP_011521790.1:p.Ser379Thr
XM_011523489.1:c.1135T>A	XP_011521791.1:p.Ser379Thr
NM_001317184.1:c.1687T>A	NP_001304113.1:p.Ser563Thr
NM_001317185.1:c.322T>A	NP_001304114.1:p.Ser108Thr
NM_001317186.1:c.-96T>A	NP_001304115.1:n.-96T>A
NM_004360.4:c.1870T>A	NP_004351.1:p.Ser624Thr
NM_004360.5:c.1870T>A MANE Select	NP_004351.1:p.Ser624Thr
NM_001317184.2:c.1687T>A	NP_001304113.1:p.Ser563Thr
NM_001317185.2:c.322T>A	NP_001304114.1:p.Ser108Thr
NM_001317186.2:c.-96T>A	NP_001304115.1:n.-96T>A