Canonical Allele Identifier: CA723146556
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs553402231
gnomAD v3: 16-68833601-GA-G
gnomAD v4: 16-68833601-GA-G
MyVariant Identifiers: chr16:g.68867505del (hg19) chr16:g.68833602del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833609del , CM000678.2:g.68833609del GRCh38
NC_000016.9:g.68867512del , CM000678.1:g.68867512del GRCh37
NC_000016.8:g.67425013del NCBI36
NG_008021.1:g.101318del , LRG_301:g.101318del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*110del MANE Select ENSP00000261769.4:n.*110del
ENST00000261769.9:c.*110del ENSP00000261769.4:n.*110del
ENST00000566612.5:c.*999del ENSP00000454782.1:n.*999del
ENST00000611625.4:c.*110del ENSP00000481063.1:n.*110del
ENST00000612417.4:c.1854-582del ENSP00000478360.1:n.1854-582del
ENST00000621016.4:c.1866-594del ENSP00000480664.1:n.1866-594del
NM_004360.3:c.*110del , LRG_301t1:c.*110del NP_004351.1:n.*110del
XM_011523488.1:c.*110del XP_011521790.1:n.*110del
XM_011523489.1:c.*110del XP_011521791.1:n.*110del
NM_001317184.1:c.*110del NP_001304113.1:n.*110del
NM_001317185.1:c.*110del NP_001304114.1:n.*110del
NM_001317186.1:c.*110del NP_001304115.1:n.*110del
NM_004360.4:c.*110del NP_004351.1:n.*110del
NM_004360.5:c.*110del MANE Select NP_004351.1:n.*110del
NM_001317184.2:c.*110del NP_001304113.1:n.*110del
NM_001317185.2:c.*110del NP_001304114.1:n.*110del
NM_001317186.2:c.*110del NP_001304115.1:n.*110del
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