Canonical Allele Identifier: CA2633932098
Gene: CDH1 HGNC NCBI

Linked Data

gnomAD v4: 16-68829942-TC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829943del , CM000678.2:g.68829943del GRCh38
NC_000016.9:g.68863846del , CM000678.1:g.68863846del GRCh37
NC_000016.8:g.67421347del NCBI36
NG_008021.1:g.97652del , LRG_301:g.97652del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+146del MANE Select ENSP00000261769.4:n.2439+146del
ENST00000261769.9:c.2439+146del ENSP00000261769.4:n.2439+146del
ENST00000422392.6:c.2256+146del ENSP00000414946.2:n.2256+146del
ENST00000562118.1:n.657+146del
ENST00000562836.5:n.2510+146del
ENST00000566510.5:c.*1105+146del ENSP00000458139.1:n.*1105+146del
ENST00000566612.5:c.*679+146del ENSP00000454782.1:n.*679+146del
ENST00000611625.4:c.2502+146del ENSP00000481063.1:n.2502+146del
ENST00000612417.4:c.1853+3389del ENSP00000478360.1:n.1853+3389del
ENST00000621016.4:c.1866-4260del ENSP00000480664.1:n.1866-4260del
NM_004360.3:c.2439+146del , LRG_301t1:c.2439+146del NP_004351.1:n.2439+146del
XM_011523488.1:c.1704+146del XP_011521790.1:n.1704+146del
XM_011523489.1:c.1704+146del XP_011521791.1:n.1704+146del
NM_001317184.1:c.2256+146del NP_001304113.1:n.2256+146del
NM_001317185.1:c.891+146del NP_001304114.1:n.891+146del
NM_001317186.1:c.474+146del NP_001304115.1:n.474+146del
NM_004360.4:c.2439+146del NP_004351.1:n.2439+146del
NM_004360.5:c.2439+146del MANE Select NP_004351.1:n.2439+146del
NM_001317184.2:c.2256+146del NP_001304113.1:n.2256+146del
NM_001317185.2:c.891+146del NP_001304114.1:n.891+146del
NM_001317186.2:c.474+146del NP_001304115.1:n.474+146del
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