Canonical Allele Identifier: CA396451565
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1801544
ClinVar RCV Id: RCV003164577
dbSNP Id: rs2152114329

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738296G>C , CM000678.2:g.68738296G>C GRCh38
NC_000016.9:g.68772199G>C , CM000678.1:g.68772199G>C GRCh37
NC_000016.8:g.67329700G>C NCBI36
NG_008021.1:g.6005G>C , LRG_301:g.6005G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.49-1G>C MANE Select ENSP00000261769.4:n.49-1G>C
ENST00000261769.9:c.49-1G>C ENSP00000261769.4:n.49-1G>C
ENST00000422392.6:c.49-1G>C ENSP00000414946.2:n.49-1G>C
ENST00000566510.5:c.49-1G>C ENSP00000458139.1:n.49-1G>C
ENST00000566612.5:c.49-1G>C ENSP00000454782.1:n.49-1G>C
ENST00000611625.4:c.49-1G>C ENSP00000481063.1:n.49-1G>C
ENST00000612417.4:c.49-1G>C ENSP00000478360.1:n.49-1G>C
ENST00000621016.4:c.49-1G>C ENSP00000480664.1:n.49-1G>C
NM_004360.3:c.49-1G>C , LRG_301t1:c.49-1G>C NP_004351.1:n.49-1G>C
NM_001317184.1:c.49-1G>C NP_001304113.1:n.49-1G>C
NM_001317185.1:c.-1567-1G>C NP_001304114.1:n.-1567-1G>C
NM_001317186.1:c.-1771-1G>C NP_001304115.1:n.-1771-1G>C
NM_004360.4:c.49-1G>C NP_004351.1:n.49-1G>C
NM_004360.5:c.49-1G>C MANE Select NP_004351.1:n.49-1G>C
NM_001317184.2:c.49-1G>C NP_001304113.1:n.49-1G>C
NM_001317185.2:c.-1567-1G>C NP_001304114.1:n.-1567-1G>C
NM_001317186.2:c.-1771-1G>C NP_001304115.1:n.-1771-1G>C