Canonical Allele Identifier: CA396458599
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3224187
ClinVar RCV Id: RCV004518913
gnomAD v4: 16-68810264-T-C
MyVariant Identifiers: chr16:g.68844167T>C (hg19) chr16:g.68810264T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810264T>C , CM000678.2:g.68810264T>C GRCh38
NC_000016.9:g.68844167T>C , CM000678.1:g.68844167T>C GRCh37
NC_000016.8:g.67401668T>C NCBI36
NG_008021.1:g.77973T>C , LRG_301:g.77973T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.755T>C MANE Select ENSP00000261769.4:p.Val252Ala
ENST00000261769.9:c.755T>C ENSP00000261769.4:p.Val252Ala
ENST00000422392.6:c.755T>C ENSP00000414946.2:p.Val252Ala
ENST00000561751.1:c.454+1416T>C
ENST00000562836.5:n.826T>C
ENST00000566510.5:c.599T>C ENSP00000458139.1:p.Val200Ala
ENST00000566612.5:c.755T>C ENSP00000454782.1:p.Val252Ala
ENST00000611625.4:c.755T>C ENSP00000481063.1:p.Val252Ala
ENST00000612417.4:c.755T>C ENSP00000478360.1:p.Val252Ala
ENST00000621016.4:c.755T>C ENSP00000480664.1:p.Val252Ala
NM_004360.3:c.755T>C , LRG_301t1:c.755T>C NP_004351.1:p.Val252Ala
XM_011523488.1:c.20T>C XP_011521790.1:p.Val7Ala
XM_011523489.1:c.20T>C XP_011521791.1:p.Val7Ala
NM_001317184.1:c.755T>C NP_001304113.1:p.Val252Ala
NM_001317185.1:c.-861T>C NP_001304114.1:n.-861T>C
NM_001317186.1:c.-1065T>C NP_001304115.1:n.-1065T>C
NM_004360.4:c.755T>C NP_004351.1:p.Val252Ala
NM_004360.5:c.755T>C MANE Select NP_004351.1:p.Val252Ala
NM_001317184.2:c.755T>C NP_001304113.1:p.Val252Ala
NM_001317185.2:c.-861T>C NP_001304114.1:n.-861T>C
NM_001317186.2:c.-1065T>C NP_001304115.1:n.-1065T>C
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