Canonical Allele Identifier: CA396458902
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1762081
ClinVar RCV Id: RCV002421286
dbSNP Id: rs2152131174
MyVariant Identifiers: chr16:g.68844223G>A (hg19) chr16:g.68810320G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810320G>A , CM000678.2:g.68810320G>A GRCh38
NC_000016.9:g.68844223G>A , CM000678.1:g.68844223G>A GRCh37
NC_000016.8:g.67401724G>A NCBI36
NG_008021.1:g.78029G>A , LRG_301:g.78029G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.811G>A MANE Select ENSP00000261769.4:p.Val271Ile
ENST00000261769.9:c.811G>A ENSP00000261769.4:p.Val271Ile
ENST00000422392.6:c.811G>A ENSP00000414946.2:p.Val271Ile
ENST00000561751.1:c.455-1364G>A
ENST00000562836.5:n.882G>A
ENST00000566510.5:c.655G>A ENSP00000458139.1:p.Val219Ile
ENST00000566612.5:c.811G>A ENSP00000454782.1:p.Val271Ile
ENST00000611625.4:c.811G>A ENSP00000481063.1:p.Val271Ile
ENST00000612417.4:c.811G>A ENSP00000478360.1:p.Val271Ile
ENST00000621016.4:c.811G>A ENSP00000480664.1:p.Val271Ile
NM_004360.3:c.811G>A , LRG_301t1:c.811G>A NP_004351.1:p.Val271Ile
XM_011523488.1:c.76G>A XP_011521790.1:p.Val26Ile
XM_011523489.1:c.76G>A XP_011521791.1:p.Val26Ile
NM_001317184.1:c.811G>A NP_001304113.1:p.Val271Ile
NM_001317185.1:c.-805G>A NP_001304114.1:n.-805G>A
NM_001317186.1:c.-1009G>A NP_001304115.1:n.-1009G>A
NM_004360.4:c.811G>A NP_004351.1:p.Val271Ile
NM_004360.5:c.811G>A MANE Select NP_004351.1:p.Val271Ile
NM_001317184.2:c.811G>A NP_001304113.1:p.Val271Ile
NM_001317185.2:c.-805G>A NP_001304114.1:n.-805G>A
NM_001317186.2:c.-1009G>A NP_001304115.1:n.-1009G>A
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