Canonical Allele Identifier: CA396451336
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 532470
ClinVar RCV Id: RCV000639268 RCV002440262
dbSNP Id: rs1555509645
MyVariant Identifiers: chr16:g.68771343T>G (hg19) chr16:g.68737440T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737440T>G , CM000678.2:g.68737440T>G GRCh38
NC_000016.9:g.68771343T>G , CM000678.1:g.68771343T>G GRCh37
NC_000016.8:g.67328844T>G NCBI36
NG_008021.1:g.5149T>G , LRG_301:g.5149T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.25T>G MANE Select ENSP00000261769.4:p.Ser9Ala
ENST00000261769.9:c.25T>G ENSP00000261769.4:p.Ser9Ala
ENST00000422392.6:c.25T>G ENSP00000414946.2:p.Ser9Ala
ENST00000566510.5:c.25T>G ENSP00000458139.1:p.Ser9Ala
ENST00000566612.5:c.25T>G ENSP00000454782.1:p.Ser9Ala
ENST00000611625.4:c.25T>G ENSP00000481063.1:p.Ser9Ala
ENST00000612417.4:c.25T>G ENSP00000478360.1:p.Ser9Ala
ENST00000621016.4:c.25T>G ENSP00000480664.1:p.Ser9Ala
NM_004360.3:c.25T>G , LRG_301t1:c.25T>G NP_004351.1:p.Ser9Ala
NM_001317184.1:c.25T>G NP_001304113.1:p.Ser9Ala
NM_001317185.1:c.-1591T>G NP_001304114.1:n.-1591T>G
NM_001317186.1:c.-1795T>G NP_001304115.1:n.-1795T>G
NM_004360.4:c.25T>G NP_004351.1:p.Ser9Ala
NM_004360.5:c.25T>G MANE Select NP_004351.1:p.Ser9Ala
NM_001317184.2:c.25T>G NP_001304113.1:p.Ser9Ala
NM_001317185.2:c.-1591T>G NP_001304114.1:n.-1591T>G
NM_001317186.2:c.-1795T>G NP_001304115.1:n.-1795T>G
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