Canonical Allele Identifier: CA2633932429
Gene: CDH1 HGNC NCBI

Linked Data

gnomAD v4: 16-68833568-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833568T>G , CM000678.2:g.68833568T>G GRCh38
NC_000016.9:g.68867471T>G , CM000678.1:g.68867471T>G GRCh37
NC_000016.8:g.67424972T>G NCBI36
NG_008021.1:g.101277T>G , LRG_301:g.101277T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*69T>G MANE Select ENSP00000261769.4:n.*69T>G
ENST00000261769.9:c.*69T>G ENSP00000261769.4:n.*69T>G
ENST00000562118.1:n.936T>G
ENST00000566612.5:c.*958T>G ENSP00000454782.1:n.*958T>G
ENST00000611625.4:c.*69T>G ENSP00000481063.1:n.*69T>G
ENST00000612417.4:c.1854-623T>G ENSP00000478360.1:n.1854-623T>G
ENST00000621016.4:c.1866-635T>G ENSP00000480664.1:n.1866-635T>G
NM_004360.3:c.*69T>G , LRG_301t1:c.*69T>G NP_004351.1:n.*69T>G
XM_011523488.1:c.*69T>G XP_011521790.1:n.*69T>G
XM_011523489.1:c.*69T>G XP_011521791.1:n.*69T>G
NM_001317184.1:c.*69T>G NP_001304113.1:n.*69T>G
NM_001317185.1:c.*69T>G NP_001304114.1:n.*69T>G
NM_001317186.1:c.*69T>G NP_001304115.1:n.*69T>G
NM_004360.4:c.*69T>G NP_004351.1:n.*69T>G
NM_004360.5:c.*69T>G MANE Select NP_004351.1:n.*69T>G
NM_001317184.2:c.*69T>G NP_001304113.1:n.*69T>G
NM_001317185.2:c.*69T>G NP_001304114.1:n.*69T>G
NM_001317186.2:c.*69T>G NP_001304115.1:n.*69T>G
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