Canonical Allele Identifier: CA2739266856
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2819810
ClinVar RCV Id: RCV003625316
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810185T>G , CM000678.2:g.68810185T>G GRCh38
NC_000016.9:g.68844088T>G , CM000678.1:g.68844088T>G GRCh37
NC_000016.8:g.67401589T>G NCBI36
NG_008021.1:g.77894T>G , LRG_301:g.77894T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.688-12T>G MANE Select ENSP00000261769.4:n.688-12T>G
ENST00000261769.9:c.688-12T>G ENSP00000261769.4:n.688-12T>G
ENST00000422392.6:c.688-12T>G ENSP00000414946.2:n.688-12T>G
ENST00000561751.1:c.454+1337T>G
ENST00000562836.5:n.759-12T>G
ENST00000566510.5:c.532-12T>G ENSP00000458139.1:n.532-12T>G
ENST00000566612.5:c.688-12T>G ENSP00000454782.1:n.688-12T>G
ENST00000611625.4:c.688-12T>G ENSP00000481063.1:n.688-12T>G
ENST00000612417.4:c.688-12T>G ENSP00000478360.1:n.688-12T>G
ENST00000621016.4:c.688-12T>G ENSP00000480664.1:n.688-12T>G
NM_004360.3:c.688-12T>G , LRG_301t1:c.688-12T>G NP_004351.1:n.688-12T>G
XM_011523488.1:c.-48-12T>G XP_011521790.1:n.-48-12T>G
XM_011523489.1:c.-48-12T>G XP_011521791.1:n.-48-12T>G
NM_001317184.1:c.688-12T>G NP_001304113.1:n.688-12T>G
NM_001317185.1:c.-928-12T>G NP_001304114.1:n.-928-12T>G
NM_001317186.1:c.-1132-12T>G NP_001304115.1:n.-1132-12T>G
NM_004360.4:c.688-12T>G NP_004351.1:n.688-12T>G
NM_004360.5:c.688-12T>G MANE Select NP_004351.1:n.688-12T>G
NM_001317184.2:c.688-12T>G NP_001304113.1:n.688-12T>G
NM_001317185.2:c.-928-12T>G NP_001304114.1:n.-928-12T>G
NM_001317186.2:c.-1132-12T>G NP_001304115.1:n.-1132-12T>G
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