Canonical Allele Identifier: CA1139664758

Gene: CDH1

Linked Data

• ClinVar Variation Id: 920881
• ClinVar RCV Id: RCV001179933
• dbSNP Id: rs1960956644

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815501T>C , CM000678.2:g.68815501T>C	GRCh38
NC_000016.9:g.68849404T>C , CM000678.1:g.68849404T>C	GRCh37
NC_000016.8:g.67406905T>C	NCBI36
NG_008021.1:g.83210T>C , LRG_301:g.83210T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1321-14T>C MANE Select	ENSP00000261769.4:n.1321-14T>C
ENST00000261769.9:c.1321-14T>C	ENSP00000261769.4:n.1321-14T>C
ENST00000422392.6:c.1138-14T>C	ENSP00000414946.2:n.1138-14T>C
ENST00000562836.5:n.1392-14T>C
ENST00000566510.5:c.1232-14T>C	ENSP00000458139.1:n.1232-14T>C
ENST00000566612.5:c.1321-14T>C	ENSP00000454782.1:n.1321-14T>C
ENST00000611625.4:c.1384-14T>C	ENSP00000481063.1:n.1384-14T>C
ENST00000612417.4:c.1321-14T>C	ENSP00000478360.1:n.1321-14T>C
ENST00000621016.4:c.1321-14T>C	ENSP00000480664.1:n.1321-14T>C
NM_004360.3:c.1321-14T>C , LRG_301t1:c.1321-14T>C	NP_004351.1:n.1321-14T>C
XM_011523488.1:c.586-14T>C	XP_011521790.1:n.586-14T>C
XM_011523489.1:c.586-14T>C	XP_011521791.1:n.586-14T>C
NM_001317184.1:c.1138-14T>C	NP_001304113.1:n.1138-14T>C
NM_001317185.1:c.-228-14T>C	NP_001304114.1:n.-228-14T>C
NM_001317186.1:c.-499-14T>C	NP_001304115.1:n.-499-14T>C
NM_004360.4:c.1321-14T>C	NP_004351.1:n.1321-14T>C
NM_004360.5:c.1321-14T>C MANE Select	NP_004351.1:n.1321-14T>C
NM_001317184.2:c.1138-14T>C	NP_001304113.1:n.1138-14T>C
NM_001317185.2:c.-228-14T>C	NP_001304114.1:n.-228-14T>C
NM_001317186.2:c.-499-14T>C	NP_001304115.1:n.-499-14T>C