Canonical Allele Identifier: CA2229975436
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1270653071

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829942dup , CM000678.2:g.68829942dup GRCh38
NC_000016.9:g.68863845dup , CM000678.1:g.68863845dup GRCh37
NC_000016.8:g.67421346dup NCBI36
NG_008021.1:g.97651dup , LRG_301:g.97651dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+145dup MANE Select ENSP00000261769.4:n.2439+145dup
ENST00000261769.9:c.2439+145dup ENSP00000261769.4:n.2439+145dup
ENST00000422392.6:c.2256+145dup ENSP00000414946.2:n.2256+145dup
ENST00000562118.1:n.657+145dup
ENST00000562836.5:n.2510+145dup
ENST00000566510.5:c.*1105+145dup ENSP00000458139.1:n.*1105+145dup
ENST00000566612.5:c.*679+145dup ENSP00000454782.1:n.*679+145dup
ENST00000611625.4:c.2502+145dup ENSP00000481063.1:n.2502+145dup
ENST00000612417.4:c.1853+3388dup ENSP00000478360.1:n.1853+3388dup
ENST00000621016.4:c.1866-4261dup ENSP00000480664.1:n.1866-4261dup
NM_004360.3:c.2439+145dup , LRG_301t1:c.2439+145dup NP_004351.1:n.2439+145dup
XM_011523488.1:c.1704+145dup XP_011521790.1:n.1704+145dup
XM_011523489.1:c.1704+145dup XP_011521791.1:n.1704+145dup
NM_001317184.1:c.2256+145dup NP_001304113.1:n.2256+145dup
NM_001317185.1:c.891+145dup NP_001304114.1:n.891+145dup
NM_001317186.1:c.474+145dup NP_001304115.1:n.474+145dup
NM_004360.4:c.2439+145dup NP_004351.1:n.2439+145dup
NM_004360.5:c.2439+145dup MANE Select NP_004351.1:n.2439+145dup
NM_001317184.2:c.2256+145dup NP_001304113.1:n.2256+145dup
NM_001317185.2:c.891+145dup NP_001304114.1:n.891+145dup
NM_001317186.2:c.474+145dup NP_001304115.1:n.474+145dup