Canonical Allele Identifier: CA396472857

Gene: CDH1

Linked Data

• ClinVar Variation Id: 3224182
• ClinVar RCV Id: RCV004518908
• dbSNP Id: rs555842031
• MyVariant Identifiers: chr16:g.68867382G>T (hg19) ; chr16:g.68833479G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833479G>T , CM000678.2:g.68833479G>T	GRCh38
NC_000016.9:g.68867382G>T , CM000678.1:g.68867382G>T	GRCh37
NC_000016.8:g.67424883G>T	NCBI36
NG_008021.1:g.101188G>T , LRG_301:g.101188G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2629G>T MANE Select	ENSP00000261769.4:p.Gly877Ter
ENST00000261769.9:c.2629G>T	ENSP00000261769.4:p.Gly877Ter
ENST00000422392.6:c.2446G>T	ENSP00000414946.2:p.Gly816Ter
ENST00000562118.1:n.847G>T
ENST00000562836.5:n.2700G>T
ENST00000566510.5:c.*1295G>T	ENSP00000458139.1:n.*1295G>T
ENST00000566612.5:c.*869G>T	ENSP00000454782.1:n.*869G>T
ENST00000611625.4:c.2692G>T	ENSP00000481063.1:p.Gly898Ter
ENST00000612417.4:c.1854-712G>T	ENSP00000478360.1:n.1854-712G>T
ENST00000621016.4:c.1866-724G>T	ENSP00000480664.1:n.1866-724G>T
NM_004360.3:c.2629G>T , LRG_301t1:c.2629G>T	NP_004351.1:p.Gly877Ter
XM_011523488.1:c.1894G>T	XP_011521790.1:p.Gly632Ter
XM_011523489.1:c.1894G>T	XP_011521791.1:p.Gly632Ter
NM_001317184.1:c.2446G>T	NP_001304113.1:p.Gly816Ter
NM_001317185.1:c.1081G>T	NP_001304114.1:p.Gly361Ter
NM_001317186.1:c.664G>T	NP_001304115.1:p.Gly222Ter
NM_004360.4:c.2629G>T	NP_004351.1:p.Gly877Ter
NM_004360.5:c.2629G>T MANE Select	NP_004351.1:p.Gly877Ter
NM_001317184.2:c.2446G>T	NP_001304113.1:p.Gly816Ter
NM_001317185.2:c.1081G>T	NP_001304114.1:p.Gly361Ter
NM_001317186.2:c.664G>T	NP_001304115.1:p.Gly222Ter