Canonical Allele Identifier: CA496154295
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 576403
ClinVar RCV Id: RCV000698885 RCV002397435
dbSNP Id: rs1555516521
gnomAD v4: 16-68819280-A-T
MyVariant Identifiers: chr16:g.68853183A>T (hg19) chr16:g.68819280A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819280A>T , CM000678.2:g.68819280A>T GRCh38
NC_000016.9:g.68853183A>T , CM000678.1:g.68853183A>T GRCh37
NC_000016.8:g.67410684A>T NCBI36
NG_008021.1:g.86989A>T , LRG_301:g.86989A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1566A>T MANE Select ENSP00000261769.4:p.Thr522=
ENST00000261769.9:c.1566A>T ENSP00000261769.4:p.Thr522=
ENST00000422392.6:c.1383A>T ENSP00000414946.2:p.Thr461=
ENST00000562836.5:n.1637A>T
ENST00000566510.5:c.*232A>T ENSP00000458139.1:n.*232A>T
ENST00000566612.5:c.1566-2721A>T ENSP00000454782.1:n.1566-2721A>T
ENST00000611625.4:c.1629A>T ENSP00000481063.1:p.Thr543=
ENST00000612417.4:c.1566A>T ENSP00000478360.1:p.Thr522=
ENST00000621016.4:c.1566A>T ENSP00000480664.1:p.Thr522=
NM_004360.3:c.1566A>T , LRG_301t1:c.1566A>T NP_004351.1:p.Thr522=
XM_011523488.1:c.831A>T XP_011521790.1:p.Thr277=
XM_011523489.1:c.831A>T XP_011521791.1:p.Thr277=
NM_001317184.1:c.1383A>T NP_001304113.1:p.Thr461=
NM_001317185.1:c.18A>T NP_001304114.1:p.Thr6=
NM_001317186.1:c.-254-2721A>T NP_001304115.1:n.-254-2721A>T
NM_004360.4:c.1566A>T NP_004351.1:p.Thr522=
NM_004360.5:c.1566A>T MANE Select NP_004351.1:p.Thr522=
NM_001317184.2:c.1383A>T NP_001304113.1:p.Thr461=
NM_001317185.2:c.18A>T NP_001304114.1:p.Thr6=
NM_001317186.2:c.-254-2721A>T NP_001304115.1:n.-254-2721A>T
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