Canonical Allele Identifier: CA396467160

Gene: CDH1

Linked Data

• dbSNP Id: rs1961168795
• MyVariant Identifiers: chr16:g.68856086C>G (hg19) ; chr16:g.68822183C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822183C>G , CM000678.2:g.68822183C>G	GRCh38
NC_000016.9:g.68856086C>G , CM000678.1:g.68856086C>G	GRCh37
NC_000016.8:g.67413587C>G	NCBI36
NG_008021.1:g.89892C>G , LRG_301:g.89892C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1894C>G MANE Select	ENSP00000261769.4:p.His632Asp
ENST00000261769.9:c.1894C>G	ENSP00000261769.4:p.His632Asp
ENST00000422392.6:c.1711C>G	ENSP00000414946.2:p.His571Asp
ENST00000562836.5:n.1965C>G
ENST00000566510.5:c.*560C>G	ENSP00000458139.1:n.*560C>G
ENST00000566612.5:c.*134C>G	ENSP00000454782.1:n.*134C>G
ENST00000611625.4:c.1957C>G	ENSP00000481063.1:p.His653Asp
ENST00000612417.4:c.1830+64C>G	ENSP00000478360.1:n.1830+64C>G
ENST00000621016.4:c.1865+29C>G	ENSP00000480664.1:n.1865+29C>G
NM_004360.3:c.1894C>G , LRG_301t1:c.1894C>G	NP_004351.1:p.His632Asp
XM_011523488.1:c.1159C>G	XP_011521790.1:p.His387Asp
XM_011523489.1:c.1159C>G	XP_011521791.1:p.His387Asp
NM_001317184.1:c.1711C>G	NP_001304113.1:p.His571Asp
NM_001317185.1:c.346C>G	NP_001304114.1:p.His116Asp
NM_001317186.1:c.-72C>G	NP_001304115.1:n.-72C>G
NM_004360.4:c.1894C>G	NP_004351.1:p.His632Asp
NM_004360.5:c.1894C>G MANE Select	NP_004351.1:p.His632Asp
NM_001317184.2:c.1711C>G	NP_001304113.1:p.His571Asp
NM_001317185.2:c.346C>G	NP_001304114.1:p.His116Asp
NM_001317186.2:c.-72C>G	NP_001304115.1:n.-72C>G