Canonical Allele Identifier: CA396457504

Gene: CDH1

Linked Data

• ClinVar Variation Id: 824320
• ClinVar RCV Id: RCV001021322
• dbSNP Id: rs1597885088
• MyVariant Identifiers: chr16:g.68835795A>G (hg19) ; chr16:g.68801892A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801892A>G , CM000678.2:g.68801892A>G	GRCh38
NC_000016.9:g.68835795A>G , CM000678.1:g.68835795A>G	GRCh37
NC_000016.8:g.67393296A>G	NCBI36
NG_008021.1:g.69601A>G , LRG_301:g.69601A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.386A>G MANE Select	ENSP00000261769.4:p.Gln129Arg
ENST00000261769.9:c.386A>G	ENSP00000261769.4:p.Gln129Arg
ENST00000422392.6:c.386A>G	ENSP00000414946.2:p.Gln129Arg
ENST00000561751.1:c.153A>G
ENST00000562836.5:n.457A>G
ENST00000564676.5:n.668A>G
ENST00000564745.1:n.381A>G
ENST00000566510.5:c.386A>G	ENSP00000458139.1:p.Gln129Arg
ENST00000566612.5:c.386A>G	ENSP00000454782.1:p.Gln129Arg
ENST00000611625.4:c.386A>G	ENSP00000481063.1:p.Gln129Arg
ENST00000612417.4:c.386A>G	ENSP00000478360.1:p.Gln129Arg
ENST00000621016.4:c.386A>G	ENSP00000480664.1:p.Gln129Arg
NM_004360.3:c.386A>G , LRG_301t1:c.386A>G	NP_004351.1:p.Gln129Arg
XM_011523488.1:c.-350A>G	XP_011521790.1:n.-350A>G
XM_011523489.1:c.-350A>G	XP_011521791.1:n.-350A>G
NM_001317184.1:c.386A>G	NP_001304113.1:p.Gln129Arg
NM_001317185.1:c.-1230A>G	NP_001304114.1:n.-1230A>G
NM_001317186.1:c.-1434A>G	NP_001304115.1:n.-1434A>G
NM_004360.4:c.386A>G	NP_004351.1:p.Gln129Arg
NM_004360.5:c.386A>G MANE Select	NP_004351.1:p.Gln129Arg
NM_001317184.2:c.386A>G	NP_001304113.1:p.Gln129Arg
NM_001317185.2:c.-1230A>G	NP_001304114.1:n.-1230A>G
NM_001317186.2:c.-1434A>G	NP_001304115.1:n.-1434A>G