Canonical Allele Identifier: CA645580222
Gene: CDH1 HGNC NCBI

Linked Data

COSMIC: COSM5446458
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833462_68833463insT , CM000678.2:g.68833462_68833463insT GRCh38
NC_000016.9:g.68867365_68867366insT , CM000678.1:g.68867365_68867366insT GRCh37
NC_000016.8:g.67424866_67424867insT NCBI36
NG_008021.1:g.101171_101172insT , LRG_301:g.101171_101172insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2612_2613insT MANE Select ENSP00000261769.4:p.Lys871AsnfsTer4
ENST00000261769.9:c.2612_2613insT ENSP00000261769.4:p.Lys871AsnfsTer4
ENST00000422392.6:c.2429_2430insT ENSP00000414946.2:p.Lys810AsnfsTer4
ENST00000562118.1:n.830_831insT
ENST00000562836.5:n.2683_2684insT
ENST00000566510.5:c.*1278_*1279insT ENSP00000458139.1:n.*1278_*1279insT
ENST00000566612.5:c.*852_*853insT ENSP00000454782.1:n.*852_*853insT
ENST00000611625.4:c.2675_2676insT ENSP00000481063.1:p.Lys892AsnfsTer4
ENST00000612417.4:c.1854-729_1854-728insT ENSP00000478360.1:n.1854-729_1854-728insT
ENST00000621016.4:c.1866-741_1866-740insT ENSP00000480664.1:n.1866-741_1866-740insT
NM_004360.3:c.2612_2613insT , LRG_301t1:c.2612_2613insT NP_004351.1:p.Lys871AsnfsTer4
XM_011523488.1:c.1877_1878insT XP_011521790.1:p.Lys626AsnfsTer4
XM_011523489.1:c.1877_1878insT XP_011521791.1:p.Lys626AsnfsTer4
NM_001317184.1:c.2429_2430insT NP_001304113.1:p.Lys810AsnfsTer4
NM_001317185.1:c.1064_1065insT NP_001304114.1:p.Lys355AsnfsTer4
NM_001317186.1:c.647_648insT NP_001304115.1:p.Lys216AsnfsTer4
NM_004360.4:c.2612_2613insT NP_004351.1:p.Lys871AsnfsTer4
NM_004360.5:c.2612_2613insT MANE Select NP_004351.1:p.Lys871AsnfsTer4
NM_001317184.2:c.2429_2430insT NP_001304113.1:p.Lys810AsnfsTer4
NM_001317185.2:c.1064_1065insT NP_001304114.1:p.Lys355AsnfsTer4
NM_001317186.2:c.647_648insT NP_001304115.1:p.Lys216AsnfsTer4
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