Canonical Allele Identifier: CA913188830
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 628518
ClinVar RCV Id: RCV000772998
dbSNP Id: rs1567516245
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829816A>G , CM000678.2:g.68829816A>G GRCh38
NC_000016.9:g.68863719A>G , CM000678.1:g.68863719A>G GRCh37
NC_000016.8:g.67421220A>G NCBI36
NG_008021.1:g.97525A>G , LRG_301:g.97525A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+19A>G MANE Select ENSP00000261769.4:n.2439+19A>G
ENST00000261769.9:c.2439+19A>G ENSP00000261769.4:n.2439+19A>G
ENST00000422392.6:c.2256+19A>G ENSP00000414946.2:n.2256+19A>G
ENST00000562118.1:n.657+19A>G
ENST00000562836.5:n.2510+19A>G
ENST00000566510.5:c.*1105+19A>G ENSP00000458139.1:n.*1105+19A>G
ENST00000566612.5:c.*679+19A>G ENSP00000454782.1:n.*679+19A>G
ENST00000611625.4:c.2502+19A>G ENSP00000481063.1:n.2502+19A>G
ENST00000612417.4:c.1853+3262A>G ENSP00000478360.1:n.1853+3262A>G
ENST00000621016.4:c.1866-4387A>G ENSP00000480664.1:n.1866-4387A>G
NM_004360.3:c.2439+19A>G , LRG_301t1:c.2439+19A>G NP_004351.1:n.2439+19A>G
XM_011523488.1:c.1704+19A>G XP_011521790.1:n.1704+19A>G
XM_011523489.1:c.1704+19A>G XP_011521791.1:n.1704+19A>G
NM_001317184.1:c.2256+19A>G NP_001304113.1:n.2256+19A>G
NM_001317185.1:c.891+19A>G NP_001304114.1:n.891+19A>G
NM_001317186.1:c.474+19A>G NP_001304115.1:n.474+19A>G
NM_004360.4:c.2439+19A>G NP_004351.1:n.2439+19A>G
NM_004360.5:c.2439+19A>G MANE Select NP_004351.1:n.2439+19A>G
NM_001317184.2:c.2256+19A>G NP_001304113.1:n.2256+19A>G
NM_001317185.2:c.891+19A>G NP_001304114.1:n.891+19A>G
NM_001317186.2:c.474+19A>G NP_001304115.1:n.474+19A>G
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