Canonical Allele Identifier: CA396472184
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152143948
MyVariant Identifiers: chr16:g.68867254A>G (hg19) chr16:g.68833351A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833351A>G , CM000678.2:g.68833351A>G GRCh38
NC_000016.9:g.68867254A>G , CM000678.1:g.68867254A>G GRCh37
NC_000016.8:g.67424755A>G NCBI36
NG_008021.1:g.101060A>G , LRG_301:g.101060A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2501A>G MANE Select ENSP00000261769.4:p.Asp834Gly
ENST00000261769.9:c.2501A>G ENSP00000261769.4:p.Asp834Gly
ENST00000422392.6:c.2318A>G ENSP00000414946.2:p.Asp773Gly
ENST00000562118.1:n.719A>G
ENST00000562836.5:n.2572A>G
ENST00000566510.5:c.*1167A>G ENSP00000458139.1:n.*1167A>G
ENST00000566612.5:c.*741A>G ENSP00000454782.1:n.*741A>G
ENST00000611625.4:c.2564A>G ENSP00000481063.1:p.Asp855Gly
ENST00000612417.4:c.1854-840A>G ENSP00000478360.1:n.1854-840A>G
ENST00000621016.4:c.1866-852A>G ENSP00000480664.1:n.1866-852A>G
NM_004360.3:c.2501A>G , LRG_301t1:c.2501A>G NP_004351.1:p.Asp834Gly
XM_011523488.1:c.1766A>G XP_011521790.1:p.Asp589Gly
XM_011523489.1:c.1766A>G XP_011521791.1:p.Asp589Gly
NM_001317184.1:c.2318A>G NP_001304113.1:p.Asp773Gly
NM_001317185.1:c.953A>G NP_001304114.1:p.Asp318Gly
NM_001317186.1:c.536A>G NP_001304115.1:p.Asp179Gly
NM_004360.4:c.2501A>G NP_004351.1:p.Asp834Gly
NM_004360.5:c.2501A>G MANE Select NP_004351.1:p.Asp834Gly
NM_001317184.2:c.2318A>G NP_001304113.1:p.Asp773Gly
NM_001317185.2:c.953A>G NP_001304114.1:p.Asp318Gly
NM_001317186.2:c.536A>G NP_001304115.1:p.Asp179Gly
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