Canonical Allele Identifier: CA396471077
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68863627C>G (hg19) chr16:g.68829724C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829724C>G , CM000678.2:g.68829724C>G GRCh38
NC_000016.9:g.68863627C>G , CM000678.1:g.68863627C>G GRCh37
NC_000016.8:g.67421128C>G NCBI36
NG_008021.1:g.97433C>G , LRG_301:g.97433C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2366C>G MANE Select ENSP00000261769.4:p.Pro789Arg
ENST00000261769.9:c.2366C>G ENSP00000261769.4:p.Pro789Arg
ENST00000422392.6:c.2183C>G ENSP00000414946.2:p.Pro728Arg
ENST00000562118.1:n.584C>G
ENST00000562836.5:n.2437C>G
ENST00000566510.5:c.*1032C>G ENSP00000458139.1:n.*1032C>G
ENST00000566612.5:c.*606C>G ENSP00000454782.1:n.*606C>G
ENST00000611625.4:c.2429C>G ENSP00000481063.1:p.Pro810Arg
ENST00000612417.4:c.1853+3170C>G ENSP00000478360.1:n.1853+3170C>G
ENST00000621016.4:c.1866-4479C>G ENSP00000480664.1:n.1866-4479C>G
NM_004360.3:c.2366C>G , LRG_301t1:c.2366C>G NP_004351.1:p.Pro789Arg
XM_011523488.1:c.1631C>G XP_011521790.1:p.Pro544Arg
XM_011523489.1:c.1631C>G XP_011521791.1:p.Pro544Arg
NM_001317184.1:c.2183C>G NP_001304113.1:p.Pro728Arg
NM_001317185.1:c.818C>G NP_001304114.1:p.Pro273Arg
NM_001317186.1:c.401C>G NP_001304115.1:p.Pro134Arg
NM_004360.4:c.2366C>G NP_004351.1:p.Pro789Arg
NM_004360.5:c.2366C>G MANE Select NP_004351.1:p.Pro789Arg
NM_001317184.2:c.2183C>G NP_001304113.1:p.Pro728Arg
NM_001317185.2:c.818C>G NP_001304114.1:p.Pro273Arg
NM_001317186.2:c.401C>G NP_001304115.1:p.Pro134Arg
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