Canonical Allele Identifier: CA978527713
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1961443060

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829973_68829975del , CM000678.2:g.68829973_68829975del GRCh38
NC_000016.9:g.68863876_68863878del , CM000678.1:g.68863876_68863878del GRCh37
NC_000016.8:g.67421377_67421379del NCBI36
NG_008021.1:g.97682_97684del , LRG_301:g.97682_97684del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+176_2439+178del MANE Select ENSP00000261769.4:n.2439+176_2439+178del
ENST00000261769.9:c.2439+176_2439+178del ENSP00000261769.4:n.2439+176_2439+178del
ENST00000422392.6:c.2256+176_2256+178del ENSP00000414946.2:n.2256+176_2256+178del
ENST00000562118.1:n.657+176_657+178del
ENST00000562836.5:n.2510+176_2510+178del
ENST00000566510.5:c.*1105+176_*1105+178del ENSP00000458139.1:n.*1105+176_*1105+178del
ENST00000566612.5:c.*679+176_*679+178del ENSP00000454782.1:n.*679+176_*679+178del
ENST00000611625.4:c.2502+176_2502+178del ENSP00000481063.1:n.2502+176_2502+178del
ENST00000612417.4:c.1853+3419_1853+3421del ENSP00000478360.1:n.1853+3419_1853+3421del
ENST00000621016.4:c.1866-4230_1866-4228del ENSP00000480664.1:n.1866-4230_1866-4228del
NM_004360.3:c.2439+176_2439+178del , LRG_301t1:c.2439+176_2439+178del NP_004351.1:n.2439+176_2439+178del
XM_011523488.1:c.1704+176_1704+178del XP_011521790.1:n.1704+176_1704+178del
XM_011523489.1:c.1704+176_1704+178del XP_011521791.1:n.1704+176_1704+178del
NM_001317184.1:c.2256+176_2256+178del NP_001304113.1:n.2256+176_2256+178del
NM_001317185.1:c.891+176_891+178del NP_001304114.1:n.891+176_891+178del
NM_001317186.1:c.474+176_474+178del NP_001304115.1:n.474+176_474+178del
NM_004360.4:c.2439+176_2439+178del NP_004351.1:n.2439+176_2439+178del
NM_004360.5:c.2439+176_2439+178del MANE Select NP_004351.1:n.2439+176_2439+178del
NM_001317184.2:c.2256+176_2256+178del NP_001304113.1:n.2256+176_2256+178del
NM_001317185.2:c.891+176_891+178del NP_001304114.1:n.891+176_891+178del
NM_001317186.2:c.474+176_474+178del NP_001304115.1:n.474+176_474+178del