Canonical Allele Identifier: CA396472471
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1793146
ClinVar RCV Id: RCV002433420
gnomAD v4: 16-68833414-A-G
MyVariant Identifiers: chr16:g.68867317A>G (hg19) chr16:g.68833414A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833414A>G , CM000678.2:g.68833414A>G GRCh38
NC_000016.9:g.68867317A>G , CM000678.1:g.68867317A>G GRCh37
NC_000016.8:g.67424818A>G NCBI36
NG_008021.1:g.101123A>G , LRG_301:g.101123A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2564A>G MANE Select ENSP00000261769.4:p.Lys855Arg
ENST00000261769.9:c.2564A>G ENSP00000261769.4:p.Lys855Arg
ENST00000422392.6:c.2381A>G ENSP00000414946.2:p.Lys794Arg
ENST00000562118.1:n.782A>G
ENST00000562836.5:n.2635A>G
ENST00000566510.5:c.*1230A>G ENSP00000458139.1:n.*1230A>G
ENST00000566612.5:c.*804A>G ENSP00000454782.1:n.*804A>G
ENST00000611625.4:c.2627A>G ENSP00000481063.1:p.Lys876Arg
ENST00000612417.4:c.1854-777A>G ENSP00000478360.1:n.1854-777A>G
ENST00000621016.4:c.1866-789A>G ENSP00000480664.1:n.1866-789A>G
NM_004360.3:c.2564A>G , LRG_301t1:c.2564A>G NP_004351.1:p.Lys855Arg
XM_011523488.1:c.1829A>G XP_011521790.1:p.Lys610Arg
XM_011523489.1:c.1829A>G XP_011521791.1:p.Lys610Arg
NM_001317184.1:c.2381A>G NP_001304113.1:p.Lys794Arg
NM_001317185.1:c.1016A>G NP_001304114.1:p.Lys339Arg
NM_001317186.1:c.599A>G NP_001304115.1:p.Lys200Arg
NM_004360.4:c.2564A>G NP_004351.1:p.Lys855Arg
NM_004360.5:c.2564A>G MANE Select NP_004351.1:p.Lys855Arg
NM_001317184.2:c.2381A>G NP_001304113.1:p.Lys794Arg
NM_001317185.2:c.1016A>G NP_001304114.1:p.Lys339Arg
NM_001317186.2:c.599A>G NP_001304115.1:p.Lys200Arg
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