Canonical Allele Identifier: CA723197127
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1241992746

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68802066_68802082del , CM000678.2:g.68802066_68802082del GRCh38
NC_000016.9:g.68835969_68835985del , CM000678.1:g.68835969_68835985del GRCh37
NC_000016.8:g.67393470_67393486del NCBI36
NG_008021.1:g.69775_69791del , LRG_301:g.69775_69791del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.387+173_387+189del MANE Select ENSP00000261769.4:n.387+173_387+189del
ENST00000261769.9:c.387+173_387+189del ENSP00000261769.4:n.387+173_387+189del
ENST00000422392.6:c.387+173_387+189del ENSP00000414946.2:n.387+173_387+189del
ENST00000561751.1:c.154+173_154+189del
ENST00000562836.5:n.458+173_458+189del
ENST00000564676.5:n.669+173_669+189del
ENST00000564745.1:n.382+173_382+189del
ENST00000566510.5:c.387+173_387+189del ENSP00000458139.1:n.387+173_387+189del
ENST00000566612.5:c.387+173_387+189del ENSP00000454782.1:n.387+173_387+189del
ENST00000611625.4:c.387+173_387+189del ENSP00000481063.1:n.387+173_387+189del
ENST00000612417.4:c.387+173_387+189del ENSP00000478360.1:n.387+173_387+189del
ENST00000621016.4:c.387+173_387+189del ENSP00000480664.1:n.387+173_387+189del
NM_004360.3:c.387+173_387+189del , LRG_301t1:c.387+173_387+189del NP_004351.1:n.387+173_387+189del
XM_011523488.1:c.-349+173_-349+189del XP_011521790.1:n.-349+173_-349+189del
XM_011523489.1:c.-349+173_-349+189del XP_011521791.1:n.-349+173_-349+189del
NM_001317184.1:c.387+173_387+189del NP_001304113.1:n.387+173_387+189del
NM_001317185.1:c.-1229+173_-1229+189del NP_001304114.1:n.-1229+173_-1229+189del
NM_001317186.1:c.-1433+173_-1433+189del NP_001304115.1:n.-1433+173_-1433+189del
NM_004360.4:c.387+173_387+189del NP_004351.1:n.387+173_387+189del
NM_004360.5:c.387+173_387+189del MANE Select NP_004351.1:n.387+173_387+189del
NM_001317184.2:c.387+173_387+189del NP_001304113.1:n.387+173_387+189del
NM_001317185.2:c.-1229+173_-1229+189del NP_001304114.1:n.-1229+173_-1229+189del
NM_001317186.2:c.-1433+173_-1433+189del NP_001304115.1:n.-1433+173_-1433+189del