Canonical Allele Identifier: CA2732902137
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152113896

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737378A>T , CM000678.2:g.68737378A>T GRCh38
NC_000016.9:g.68771281A>T , CM000678.1:g.68771281A>T GRCh37
NC_000016.8:g.67328782A>T NCBI36
NG_008021.1:g.5087A>T , LRG_301:g.5087A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-38A>T MANE Select ENSP00000261769.4:n.-38A>T
ENST00000261769.9:c.-38A>T ENSP00000261769.4:n.-38A>T
ENST00000422392.6:c.-38A>T ENSP00000414946.2:n.-38A>T
ENST00000566510.5:c.-38A>T ENSP00000458139.1:n.-38A>T
ENST00000566612.5:c.-38A>T ENSP00000454782.1:n.-38A>T
ENST00000611625.4:c.-38A>T ENSP00000481063.1:n.-38A>T
ENST00000612417.4:c.-38A>T ENSP00000478360.1:n.-38A>T
ENST00000621016.4:c.-38A>T ENSP00000480664.1:n.-38A>T
NM_004360.3:c.-38A>T , LRG_301t1:c.-38A>T NP_004351.1:n.-38A>T
NM_001317184.1:c.-38A>T NP_001304113.1:n.-38A>T
NM_001317185.1:c.-1653A>T NP_001304114.1:n.-1653A>T
NM_001317186.1:c.-1857A>T NP_001304115.1:n.-1857A>T
NM_004360.4:c.-38A>T NP_004351.1:n.-38A>T
NM_004360.5:c.-38A>T MANE Select NP_004351.1:n.-38A>T
NM_001317184.2:c.-38A>T NP_001304113.1:n.-38A>T
NM_001317185.2:c.-1653A>T NP_001304114.1:n.-1653A>T
NM_001317186.2:c.-1857A>T NP_001304115.1:n.-1857A>T