Canonical Allele Identifier: CA396472846
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs778681919
MyVariant Identifiers: chr16:g.68867381C>G (hg19) chr16:g.68833478C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833478C>G , CM000678.2:g.68833478C>G GRCh38
NC_000016.9:g.68867381C>G , CM000678.1:g.68867381C>G GRCh37
NC_000016.8:g.67424882C>G NCBI36
NG_008021.1:g.101187C>G , LRG_301:g.101187C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2628C>G MANE Select ENSP00000261769.4:p.Tyr876Ter
ENST00000261769.9:c.2628C>G ENSP00000261769.4:p.Tyr876Ter
ENST00000422392.6:c.2445C>G ENSP00000414946.2:p.Tyr815Ter
ENST00000562118.1:n.846C>G
ENST00000562836.5:n.2699C>G
ENST00000566510.5:c.*1294C>G ENSP00000458139.1:n.*1294C>G
ENST00000566612.5:c.*868C>G ENSP00000454782.1:n.*868C>G
ENST00000611625.4:c.2691C>G ENSP00000481063.1:p.Tyr897Ter
ENST00000612417.4:c.1854-713C>G ENSP00000478360.1:n.1854-713C>G
ENST00000621016.4:c.1866-725C>G ENSP00000480664.1:n.1866-725C>G
NM_004360.3:c.2628C>G , LRG_301t1:c.2628C>G NP_004351.1:p.Tyr876Ter
XM_011523488.1:c.1893C>G XP_011521790.1:p.Tyr631Ter
XM_011523489.1:c.1893C>G XP_011521791.1:p.Tyr631Ter
NM_001317184.1:c.2445C>G NP_001304113.1:p.Tyr815Ter
NM_001317185.1:c.1080C>G NP_001304114.1:p.Tyr360Ter
NM_001317186.1:c.663C>G NP_001304115.1:p.Tyr221Ter
NM_004360.4:c.2628C>G NP_004351.1:p.Tyr876Ter
NM_004360.5:c.2628C>G MANE Select NP_004351.1:p.Tyr876Ter
NM_001317184.2:c.2445C>G NP_001304113.1:p.Tyr815Ter
NM_001317185.2:c.1080C>G NP_001304114.1:p.Tyr360Ter
NM_001317186.2:c.663C>G NP_001304115.1:p.Tyr221Ter
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