Canonical Allele Identifier: CA2229975495
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829953_68829961delinsCTTTTTCTT , CM000678.2:g.68829953_68829961delinsCTTTTTCTT GRCh38
NC_000016.9:g.68863856_68863864delinsCTTTTTCTT , CM000678.1:g.68863856_68863864delinsCTTTTTCTT GRCh37
NC_000016.8:g.67421357_67421365delinsCTTTTTCTT NCBI36
NG_008021.1:g.97662_97670delinsCTTTTTCTT , LRG_301:g.97662_97670delinsCTTTTTCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+156_2439+164delinsCTTTTTCTT MANE Select ENSP00000261769.4:n.2439+156_2439+164delinsCTTTTTCTT
ENST00000261769.9:c.2439+156_2439+164delinsCTTTTTCTT ENSP00000261769.4:n.2439+156_2439+164delinsCTTTTTCTT
ENST00000422392.6:c.2256+156_2256+164delinsCTTTTTCTT ENSP00000414946.2:n.2256+156_2256+164delinsCTTTTTCTT
ENST00000562118.1:n.657+156_657+164delinsCTTTTTCTT
ENST00000562836.5:n.2510+156_2510+164delinsCTTTTTCTT
ENST00000566510.5:c.*1105+156_*1105+164delinsCTTTTTCTT ENSP00000458139.1:n.*1105+156_*1105+164delinsCTTTTTCTT
ENST00000566612.5:c.*679+156_*679+164delinsCTTTTTCTT ENSP00000454782.1:n.*679+156_*679+164delinsCTTTTTCTT
ENST00000611625.4:c.2502+156_2502+164delinsCTTTTTCTT ENSP00000481063.1:n.2502+156_2502+164delinsCTTTTTCTT
ENST00000612417.4:c.1853+3399_1853+3407delinsCTTTTTCTT ENSP00000478360.1:n.1853+3399_1853+3407delinsCTTTTTCTT
ENST00000621016.4:c.1866-4250_1866-4242delinsCTTTTTCTT ENSP00000480664.1:n.1866-4250_1866-4242delinsCTTTTTCTT
NM_004360.3:c.2439+156_2439+164delinsCTTTTTCTT , LRG_301t1:c.2439+156_2439+164delinsCTTTTTCTT NP_004351.1:n.2439+156_2439+164delinsCTTTTTCTT
XM_011523488.1:c.1704+156_1704+164delinsCTTTTTCTT XP_011521790.1:n.1704+156_1704+164delinsCTTTTTCTT
XM_011523489.1:c.1704+156_1704+164delinsCTTTTTCTT XP_011521791.1:n.1704+156_1704+164delinsCTTTTTCTT
NM_001317184.1:c.2256+156_2256+164delinsCTTTTTCTT NP_001304113.1:n.2256+156_2256+164delinsCTTTTTCTT
NM_001317185.1:c.891+156_891+164delinsCTTTTTCTT NP_001304114.1:n.891+156_891+164delinsCTTTTTCTT
NM_001317186.1:c.474+156_474+164delinsCTTTTTCTT NP_001304115.1:n.474+156_474+164delinsCTTTTTCTT
NM_004360.4:c.2439+156_2439+164delinsCTTTTTCTT NP_004351.1:n.2439+156_2439+164delinsCTTTTTCTT
NM_004360.5:c.2439+156_2439+164delinsCTTTTTCTT MANE Select NP_004351.1:n.2439+156_2439+164delinsCTTTTTCTT
NM_001317184.2:c.2256+156_2256+164delinsCTTTTTCTT NP_001304113.1:n.2256+156_2256+164delinsCTTTTTCTT
NM_001317185.2:c.891+156_891+164delinsCTTTTTCTT NP_001304114.1:n.891+156_891+164delinsCTTTTTCTT
NM_001317186.2:c.474+156_474+164delinsCTTTTTCTT NP_001304115.1:n.474+156_474+164delinsCTTTTTCTT