Canonical Allele Identifier: CA396472396
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1328677
ClinVar RCV Id: RCV001797309
dbSNP Id: rs2152144054
MyVariant Identifiers: chr16:g.68867301T>G (hg19) chr16:g.68833398T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833398T>G , CM000678.2:g.68833398T>G GRCh38
NC_000016.9:g.68867301T>G , CM000678.1:g.68867301T>G GRCh37
NC_000016.8:g.67424802T>G NCBI36
NG_008021.1:g.101107T>G , LRG_301:g.101107T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2548T>G MANE Select ENSP00000261769.4:p.Ser850Ala
ENST00000261769.9:c.2548T>G ENSP00000261769.4:p.Ser850Ala
ENST00000422392.6:c.2365T>G ENSP00000414946.2:p.Ser789Ala
ENST00000562118.1:n.766T>G
ENST00000562836.5:n.2619T>G
ENST00000566510.5:c.*1214T>G ENSP00000458139.1:n.*1214T>G
ENST00000566612.5:c.*788T>G ENSP00000454782.1:n.*788T>G
ENST00000611625.4:c.2611T>G ENSP00000481063.1:p.Ser871Ala
ENST00000612417.4:c.1854-793T>G ENSP00000478360.1:n.1854-793T>G
ENST00000621016.4:c.1866-805T>G ENSP00000480664.1:n.1866-805T>G
NM_004360.3:c.2548T>G , LRG_301t1:c.2548T>G NP_004351.1:p.Ser850Ala
XM_011523488.1:c.1813T>G XP_011521790.1:p.Ser605Ala
XM_011523489.1:c.1813T>G XP_011521791.1:p.Ser605Ala
NM_001317184.1:c.2365T>G NP_001304113.1:p.Ser789Ala
NM_001317185.1:c.1000T>G NP_001304114.1:p.Ser334Ala
NM_001317186.1:c.583T>G NP_001304115.1:p.Ser195Ala
NM_004360.4:c.2548T>G NP_004351.1:p.Ser850Ala
NM_004360.5:c.2548T>G MANE Select NP_004351.1:p.Ser850Ala
NM_001317184.2:c.2365T>G NP_001304113.1:p.Ser789Ala
NM_001317185.2:c.1000T>G NP_001304114.1:p.Ser334Ala
NM_001317186.2:c.583T>G NP_001304115.1:p.Ser195Ala
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