Canonical Allele Identifier: CA2633932494
Gene: CDH1 HGNC NCBI

Linked Data

gnomAD v4: 16-68833646-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833647del , CM000678.2:g.68833647del GRCh38
NC_000016.9:g.68867550del , CM000678.1:g.68867550del GRCh37
NC_000016.8:g.67425051del NCBI36
NG_008021.1:g.101356del , LRG_301:g.101356del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*148del MANE Select ENSP00000261769.4:n.*148del
ENST00000261769.9:c.*148del ENSP00000261769.4:n.*148del
ENST00000566612.5:c.*1037del ENSP00000454782.1:n.*1037del
ENST00000611625.4:c.*148del ENSP00000481063.1:n.*148del
ENST00000612417.4:c.1854-544del ENSP00000478360.1:n.1854-544del
ENST00000621016.4:c.1866-556del ENSP00000480664.1:n.1866-556del
NM_004360.3:c.*148del , LRG_301t1:c.*148del NP_004351.1:n.*148del
XM_011523488.1:c.*148del XP_011521790.1:n.*148del
XM_011523489.1:c.*148del XP_011521791.1:n.*148del
NM_001317184.1:c.*148del NP_001304113.1:n.*148del
NM_001317185.1:c.*148del NP_001304114.1:n.*148del
NM_001317186.1:c.*148del NP_001304115.1:n.*148del
NM_004360.4:c.*148del NP_004351.1:n.*148del
NM_004360.5:c.*148del MANE Select NP_004351.1:n.*148del
NM_001317184.2:c.*148del NP_001304113.1:n.*148del
NM_001317185.2:c.*148del NP_001304114.1:n.*148del
NM_001317186.2:c.*148del NP_001304115.1:n.*148del
Search 100 bp 5'
Search 100 bp 3'