Canonical Allele Identifier: CA16620225
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 421431
dbSNP Id: rs1064795133

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737371C>T , CM000678.2:g.68737371C>T GRCh38
NC_000016.9:g.68771274C>T , CM000678.1:g.68771274C>T GRCh37
NC_000016.8:g.67328775C>T NCBI36
NG_008021.1:g.5080C>T , LRG_301:g.5080C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-45C>T MANE Select ENSP00000261769.4:n.-45C>T
ENST00000261769.9:c.-45C>T ENSP00000261769.4:n.-45C>T
ENST00000422392.6:c.-45C>T ENSP00000414946.2:n.-45C>T
ENST00000566510.5:c.-45C>T ENSP00000458139.1:n.-45C>T
ENST00000566612.5:c.-45C>T ENSP00000454782.1:n.-45C>T
ENST00000611625.4:c.-45C>T ENSP00000481063.1:n.-45C>T
ENST00000612417.4:c.-45C>T ENSP00000478360.1:n.-45C>T
ENST00000621016.4:c.-45C>T ENSP00000480664.1:n.-45C>T
NM_004360.3:c.-45C>T , LRG_301t1:c.-45C>T NP_004351.1:n.-45C>T
NM_001317184.1:c.-45C>T NP_001304113.1:n.-45C>T
NM_001317185.1:c.-1660C>T NP_001304114.1:n.-1660C>T
NM_001317186.1:c.-1864C>T NP_001304115.1:n.-1864C>T
NM_004360.4:c.-45C>T NP_004351.1:n.-45C>T
NM_004360.5:c.-45C>T MANE Select NP_004351.1:n.-45C>T
NM_001317184.2:c.-45C>T NP_001304113.1:n.-45C>T
NM_001317185.2:c.-1660C>T NP_001304114.1:n.-1660C>T
NM_001317186.2:c.-1864C>T NP_001304115.1:n.-1864C>T