Canonical Allele Identifier: CA723200434
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1405780224

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68808355_68808356insG , CM000678.2:g.68808355_68808356insG GRCh38
NC_000016.9:g.68842258_68842259insG , CM000678.1:g.68842258_68842259insG GRCh37
NC_000016.8:g.67399759_67399760insG NCBI36
NG_008021.1:g.76064_76065insG , LRG_301:g.76064_76065insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.388-69_388-68insG MANE Select ENSP00000261769.4:n.388-69_388-68insG
ENST00000261769.9:c.388-69_388-68insG ENSP00000261769.4:n.388-69_388-68insG
ENST00000422392.6:c.388-69_388-68insG ENSP00000414946.2:n.388-69_388-68insG
ENST00000561751.1:c.155-69_155-68insG
ENST00000562836.5:n.459-69_459-68insG
ENST00000564676.5:n.670-69_670-68insG
ENST00000564745.1:n.383-69_383-68insG
ENST00000566510.5:c.388-69_388-68insG ENSP00000458139.1:n.388-69_388-68insG
ENST00000566612.5:c.388-69_388-68insG ENSP00000454782.1:n.388-69_388-68insG
ENST00000611625.4:c.388-69_388-68insG ENSP00000481063.1:n.388-69_388-68insG
ENST00000612417.4:c.388-69_388-68insG ENSP00000478360.1:n.388-69_388-68insG
ENST00000621016.4:c.388-69_388-68insG ENSP00000480664.1:n.388-69_388-68insG
NM_004360.3:c.388-69_388-68insG , LRG_301t1:c.388-69_388-68insG NP_004351.1:n.388-69_388-68insG
XM_011523488.1:c.-348-69_-348-68insG XP_011521790.1:n.-348-69_-348-68insG
XM_011523489.1:c.-348-69_-348-68insG XP_011521791.1:n.-348-69_-348-68insG
NM_001317184.1:c.388-69_388-68insG NP_001304113.1:n.388-69_388-68insG
NM_001317185.1:c.-1228-69_-1228-68insG NP_001304114.1:n.-1228-69_-1228-68insG
NM_001317186.1:c.-1432-69_-1432-68insG NP_001304115.1:n.-1432-69_-1432-68insG
NM_004360.4:c.388-69_388-68insG NP_004351.1:n.388-69_388-68insG
NM_004360.5:c.388-69_388-68insG MANE Select NP_004351.1:n.388-69_388-68insG
NM_001317184.2:c.388-69_388-68insG NP_001304113.1:n.388-69_388-68insG
NM_001317185.2:c.-1228-69_-1228-68insG NP_001304114.1:n.-1228-69_-1228-68insG
NM_001317186.2:c.-1432-69_-1432-68insG NP_001304115.1:n.-1432-69_-1432-68insG