Canonical Allele Identifier: CA2732663133
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1962418098

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737344T>A , CM000678.2:g.68737344T>A GRCh38
NC_000016.9:g.68771247T>A , CM000678.1:g.68771247T>A GRCh37
NC_000016.8:g.67328748T>A NCBI36
NG_008021.1:g.5053T>A , LRG_301:g.5053T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-72T>A MANE Select ENSP00000261769.4:n.-72T>A
ENST00000261769.9:c.-72T>A ENSP00000261769.4:n.-72T>A
ENST00000566612.5:c.-72T>A ENSP00000454782.1:n.-72T>A
ENST00000611625.4:c.-72T>A ENSP00000481063.1:n.-72T>A
ENST00000612417.4:c.-72T>A ENSP00000478360.1:n.-72T>A
ENST00000621016.4:c.-72T>A ENSP00000480664.1:n.-72T>A
NM_004360.3:c.-72T>A , LRG_301t1:c.-72T>A NP_004351.1:n.-72T>A
NM_001317184.1:c.-72T>A NP_001304113.1:n.-72T>A
NM_001317185.1:c.-1687T>A NP_001304114.1:n.-1687T>A
NM_001317186.1:c.-1891T>A NP_001304115.1:n.-1891T>A
NM_004360.4:c.-72T>A NP_004351.1:n.-72T>A
NM_004360.5:c.-72T>A MANE Select NP_004351.1:n.-72T>A
NM_001317184.2:c.-72T>A NP_001304113.1:n.-72T>A
NM_001317185.2:c.-1687T>A NP_001304114.1:n.-1687T>A
NM_001317186.2:c.-1891T>A NP_001304115.1:n.-1891T>A