Canonical Allele Identifier: CA169871

Gene: CDH1

Linked Data

• ClinVar Variation Id: 142957
• ClinVar RCV Id: RCV000132448 ; RCV001233928
• dbSNP Id: rs587782850
• MyVariant Identifiers: chr16:g.68856090G>A (hg19) ; chr16:g.68822187G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822187G>A , CM000678.2:g.68822187G>A	GRCh38
NC_000016.9:g.68856090G>A , CM000678.1:g.68856090G>A	GRCh37
NC_000016.8:g.67413591G>A	NCBI36
NG_008021.1:g.89896G>A , LRG_301:g.89896G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1898G>A MANE Select	ENSP00000261769.4:p.Gly633Glu
ENST00000261769.9:c.1898G>A	ENSP00000261769.4:p.Gly633Glu
ENST00000422392.6:c.1715G>A	ENSP00000414946.2:p.Gly572Glu
ENST00000562836.5:n.1969G>A
ENST00000566510.5:c.*564G>A	ENSP00000458139.1:n.*564G>A
ENST00000566612.5:c.*138G>A	ENSP00000454782.1:n.*138G>A
ENST00000611625.4:c.1961G>A	ENSP00000481063.1:p.Gly654Glu
ENST00000612417.4:c.1830+68G>A	ENSP00000478360.1:n.1830+68G>A
ENST00000621016.4:c.1865+33G>A	ENSP00000480664.1:n.1865+33G>A
NM_004360.3:c.1898G>A , LRG_301t1:c.1898G>A	NP_004351.1:p.Gly633Glu
XM_011523488.1:c.1163G>A	XP_011521790.1:p.Gly388Glu
XM_011523489.1:c.1163G>A	XP_011521791.1:p.Gly388Glu
NM_001317184.1:c.1715G>A	NP_001304113.1:p.Gly572Glu
NM_001317185.1:c.350G>A	NP_001304114.1:p.Gly117Glu
NM_001317186.1:c.-68G>A	NP_001304115.1:n.-68G>A
NM_004360.4:c.1898G>A	NP_004351.1:p.Gly633Glu
NM_004360.5:c.1898G>A MANE Select	NP_004351.1:p.Gly633Glu
NM_001317184.2:c.1715G>A	NP_001304113.1:p.Gly572Glu
NM_001317185.2:c.350G>A	NP_001304114.1:p.Gly117Glu
NM_001317186.2:c.-68G>A	NP_001304115.1:n.-68G>A