Canonical Allele Identifier: CA396471947
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68867195T>G (hg19) chr16:g.68833292T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833292T>G , CM000678.2:g.68833292T>G GRCh38
NC_000016.9:g.68867195T>G , CM000678.1:g.68867195T>G GRCh37
NC_000016.8:g.67424696T>G NCBI36
NG_008021.1:g.101001T>G , LRG_301:g.101001T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2442T>G MANE Select ENSP00000261769.4:p.Asn814Lys
ENST00000261769.9:c.2442T>G ENSP00000261769.4:p.Asn814Lys
ENST00000422392.6:c.2259T>G ENSP00000414946.2:p.Asn753Lys
ENST00000562118.1:n.660T>G
ENST00000562836.5:n.2513T>G
ENST00000566510.5:c.*1108T>G ENSP00000458139.1:n.*1108T>G
ENST00000566612.5:c.*682T>G ENSP00000454782.1:n.*682T>G
ENST00000611625.4:c.2505T>G ENSP00000481063.1:p.Asn835Lys
ENST00000612417.4:c.1854-899T>G ENSP00000478360.1:n.1854-899T>G
ENST00000621016.4:c.1866-911T>G ENSP00000480664.1:n.1866-911T>G
NM_004360.3:c.2442T>G , LRG_301t1:c.2442T>G NP_004351.1:p.Asn814Lys
XM_011523488.1:c.1707T>G XP_011521790.1:p.Asn569Lys
XM_011523489.1:c.1707T>G XP_011521791.1:p.Asn569Lys
NM_001317184.1:c.2259T>G NP_001304113.1:p.Asn753Lys
NM_001317185.1:c.894T>G NP_001304114.1:p.Asn298Lys
NM_001317186.1:c.477T>G NP_001304115.1:p.Asn159Lys
NM_004360.4:c.2442T>G NP_004351.1:p.Asn814Lys
NM_004360.5:c.2442T>G MANE Select NP_004351.1:p.Asn814Lys
NM_001317184.2:c.2259T>G NP_001304113.1:p.Asn753Lys
NM_001317185.2:c.894T>G NP_001304114.1:p.Asn298Lys
NM_001317186.2:c.477T>G NP_001304115.1:p.Asn159Lys
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