Canonical Allele Identifier: CA2633932468
Gene: CDH1 HGNC NCBI

Linked Data

gnomAD v4: 16-68833610-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833610G>A , CM000678.2:g.68833610G>A GRCh38
NC_000016.9:g.68867513G>A , CM000678.1:g.68867513G>A GRCh37
NC_000016.8:g.67425014G>A NCBI36
NG_008021.1:g.101319G>A , LRG_301:g.101319G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*111G>A MANE Select ENSP00000261769.4:n.*111G>A
ENST00000261769.9:c.*111G>A ENSP00000261769.4:n.*111G>A
ENST00000566612.5:c.*1000G>A ENSP00000454782.1:n.*1000G>A
ENST00000611625.4:c.*111G>A ENSP00000481063.1:n.*111G>A
ENST00000612417.4:c.1854-581G>A ENSP00000478360.1:n.1854-581G>A
ENST00000621016.4:c.1866-593G>A ENSP00000480664.1:n.1866-593G>A
NM_004360.3:c.*111G>A , LRG_301t1:c.*111G>A NP_004351.1:n.*111G>A
XM_011523488.1:c.*111G>A XP_011521790.1:n.*111G>A
XM_011523489.1:c.*111G>A XP_011521791.1:n.*111G>A
NM_001317184.1:c.*111G>A NP_001304113.1:n.*111G>A
NM_001317185.1:c.*111G>A NP_001304114.1:n.*111G>A
NM_001317186.1:c.*111G>A NP_001304115.1:n.*111G>A
NM_004360.4:c.*111G>A NP_004351.1:n.*111G>A
NM_004360.5:c.*111G>A MANE Select NP_004351.1:n.*111G>A
NM_001317184.2:c.*111G>A NP_001304113.1:n.*111G>A
NM_001317185.2:c.*111G>A NP_001304114.1:n.*111G>A
NM_001317186.2:c.*111G>A NP_001304115.1:n.*111G>A
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