Canonical Allele Identifier: CA2582342554
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2583616
ClinVar RCV Id: RCV003334538
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801800delinsTT , CM000678.2:g.68801800delinsTT GRCh38
NC_000016.9:g.68835703delinsTT , CM000678.1:g.68835703delinsTT GRCh37
NC_000016.8:g.67393204delinsTT NCBI36
NG_008021.1:g.69509delinsTT , LRG_301:g.69509delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.294delinsTT MANE Select ENSP00000261769.4:p.Leu99PhefsTer?
ENST00000261769.9:c.294delinsTT ENSP00000261769.4:p.Leu99PhefsTer?
ENST00000422392.6:c.294delinsTT ENSP00000414946.2:p.Leu99PhefsTer?
ENST00000561751.1:c.61delinsTT
ENST00000562836.5:n.365delinsTT
ENST00000564676.5:n.576delinsTT
ENST00000564745.1:n.289delinsTT
ENST00000566510.5:c.294delinsTT ENSP00000458139.1:p.Leu99PhefsTer?
ENST00000566612.5:c.294delinsTT ENSP00000454782.1:p.Leu99PhefsTer?
ENST00000611625.4:c.294delinsTT ENSP00000481063.1:p.Leu99PhefsTer?
ENST00000612417.4:c.294delinsTT ENSP00000478360.1:p.Leu99PhefsTer?
ENST00000621016.4:c.294delinsTT ENSP00000480664.1:p.Leu99PhefsTer?
NM_004360.3:c.294delinsTT , LRG_301t1:c.294delinsTT NP_004351.1:p.Leu99PhefsTer?
XM_011523488.1:c.-442delinsTT XP_011521790.1:n.-442delinsTT
XM_011523489.1:c.-442delinsTT XP_011521791.1:n.-442delinsTT
NM_001317184.1:c.294delinsTT NP_001304113.1:p.Leu99PhefsTer?
NM_001317185.1:c.-1322delinsTT NP_001304114.1:n.-1322delinsTT
NM_001317186.1:c.-1526delinsTT NP_001304115.1:n.-1526delinsTT
NM_004360.4:c.294delinsTT NP_004351.1:p.Leu99PhefsTer?
NM_004360.5:c.294delinsTT MANE Select NP_004351.1:p.Leu99PhefsTer?
NM_001317184.2:c.294delinsTT NP_001304113.1:p.Leu99PhefsTer?
NM_001317185.2:c.-1322delinsTT NP_001304114.1:n.-1322delinsTT
NM_001317186.2:c.-1526delinsTT NP_001304115.1:n.-1526delinsTT
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