Canonical Allele Identifier: CA396457080
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2611786
ClinVar RCV Id: RCV003384463
gnomAD v4: 16-68801673-A-G
MyVariant Identifiers: chr16:g.68835576A>G (hg19) chr16:g.68801673A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801673A>G , CM000678.2:g.68801673A>G GRCh38
NC_000016.9:g.68835576A>G , CM000678.1:g.68835576A>G GRCh37
NC_000016.8:g.67393077A>G NCBI36
NG_008021.1:g.69382A>G , LRG_301:g.69382A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.167A>G MANE Select ENSP00000261769.4:p.Asn56Ser
ENST00000261769.9:c.167A>G ENSP00000261769.4:p.Asn56Ser
ENST00000422392.6:c.167A>G ENSP00000414946.2:p.Asn56Ser
ENST00000562836.5:n.238A>G
ENST00000564676.5:n.449A>G
ENST00000564745.1:n.162A>G
ENST00000566510.5:c.167A>G ENSP00000458139.1:p.Asn56Ser
ENST00000566612.5:c.167A>G ENSP00000454782.1:p.Asn56Ser
ENST00000611625.4:c.167A>G ENSP00000481063.1:p.Asn56Ser
ENST00000612417.4:c.167A>G ENSP00000478360.1:p.Asn56Ser
ENST00000621016.4:c.167A>G ENSP00000480664.1:p.Asn56Ser
NM_004360.3:c.167A>G , LRG_301t1:c.167A>G NP_004351.1:p.Asn56Ser
XM_011523488.1:c.-569A>G XP_011521790.1:n.-569A>G
XM_011523489.1:c.-569A>G XP_011521791.1:n.-569A>G
NM_001317184.1:c.167A>G NP_001304113.1:p.Asn56Ser
NM_001317185.1:c.-1449A>G NP_001304114.1:n.-1449A>G
NM_001317186.1:c.-1653A>G NP_001304115.1:n.-1653A>G
NM_004360.4:c.167A>G NP_004351.1:p.Asn56Ser
NM_004360.5:c.167A>G MANE Select NP_004351.1:p.Asn56Ser
NM_001317184.2:c.167A>G NP_001304113.1:p.Asn56Ser
NM_001317185.2:c.-1449A>G NP_001304114.1:n.-1449A>G
NM_001317186.2:c.-1653A>G NP_001304115.1:n.-1653A>G
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