Canonical Allele Identifier: CA2229977891
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68832902_68832927delinsTTGGCATTTATCCTTCCAGGCCTTTC , CM000678.2:g.68832902_68832927delinsTTGGCATTTATCCTTCCAGGCCTTTC GRCh38
NC_000016.9:g.68866805_68866830delinsTTGGCATTTATCCTTCCAGGCCTTTC , CM000678.1:g.68866805_68866830delinsTTGGCATTTATCCTTCCAGGCCTTTC GRCh37
NC_000016.8:g.67424306_67424331delinsTTGGCATTTATCCTTCCAGGCCTTTC NCBI36
NG_008021.1:g.100611_100636delinsTTGGCATTTATCCTTCCAGGCCTTTC , LRG_301:g.100611_100636delinsTTGGCATTTATCCTTCCAGGCCTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2440-388_2440-363delinsTTGGCATTTATCCTTCCAGGCCTTTC MANE Select ENSP00000261769.4:n.2440-388_2440-363delinsTTGGCATTTATCCTTCCA...
ENST00000261769.9:c.2440-388_2440-363delinsTTGGCATTTATCCTTCCAGGCCTTTC ENSP00000261769.4:n.2440-388_2440-363delinsTTGGCATTTATCCTTCCA...
ENST00000422392.6:c.2257-388_2257-363delinsTTGGCATTTATCCTTCCAGGCCTTTC ENSP00000414946.2:n.2257-388_2257-363delinsTTGGCATTTATCCTTCCA...
ENST00000562118.1:n.658-388_658-363delinsTTGGCATTTATCCTTCCAGGCCTTTC
ENST00000562836.5:n.2511-388_2511-363delinsTTGGCATTTATCCTTCCAGGCCTTTC
ENST00000566510.5:c.*1106-388_*1106-363delinsTTGGCATTTATCCTTCCAGGCCTTTC ENSP00000458139.1:n.*1106-388_*1106-363delinsTTGGCATTTATCCTTC...
ENST00000566612.5:c.*680-388_*680-363delinsTTGGCATTTATCCTTCCAGGCCTTTC ENSP00000454782.1:n.*680-388_*680-363delinsTTGGCATTTATCCTTCCA...
ENST00000611625.4:c.2503-388_2503-363delinsTTGGCATTTATCCTTCCAGGCCTTTC ENSP00000481063.1:n.2503-388_2503-363delinsTTGGCATTTATCCTTCCA...
ENST00000612417.4:c.1854-1289_1854-1264delinsTTGGCATTTATCCTTCCAGGCCTTTC ENSP00000478360.1:n.1854-1289_1854-1264delinsTTGGCATTTATCCTTC...
ENST00000621016.4:c.1866-1301_1866-1276delinsTTGGCATTTATCCTTCCAGGCCTTTC ENSP00000480664.1:n.1866-1301_1866-1276delinsTTGGCATTTATCCTTC...
NM_004360.3:c.2440-388_2440-363delinsTTGGCATTTATCCTTCCAGGCCTTTC , LRG_301t1:c.2440-388_2440-363delinsTTGGCATTTATCCTTCCAGGCCTTTC NP_004351.1:n.2440-388_2440-363delinsTTGGCATTTATCCTTCCAGGCCTT...
XM_011523488.1:c.1705-388_1705-363delinsTTGGCATTTATCCTTCCAGGCCTTTC XP_011521790.1:n.1705-388_1705-363delinsTTGGCATTTATCCTTCCAGGC...
XM_011523489.1:c.1705-388_1705-363delinsTTGGCATTTATCCTTCCAGGCCTTTC XP_011521791.1:n.1705-388_1705-363delinsTTGGCATTTATCCTTCCAGGC...
NM_001317184.1:c.2257-388_2257-363delinsTTGGCATTTATCCTTCCAGGCCTTTC NP_001304113.1:n.2257-388_2257-363delinsTTGGCATTTATCCTTCCAGGC...
NM_001317185.1:c.892-388_892-363delinsTTGGCATTTATCCTTCCAGGCCTTTC NP_001304114.1:n.892-388_892-363delinsTTGGCATTTATCCTTCCAGGCCT...
NM_001317186.1:c.475-388_475-363delinsTTGGCATTTATCCTTCCAGGCCTTTC NP_001304115.1:n.475-388_475-363delinsTTGGCATTTATCCTTCCAGGCCT...
NM_004360.4:c.2440-388_2440-363delinsTTGGCATTTATCCTTCCAGGCCTTTC NP_004351.1:n.2440-388_2440-363delinsTTGGCATTTATCCTTCCAGGCCTT...
NM_004360.5:c.2440-388_2440-363delinsTTGGCATTTATCCTTCCAGGCCTTTC MANE Select NP_004351.1:n.2440-388_2440-363delinsTTGGCATTTATCCTTCCAGGCCTT...
NM_001317184.2:c.2257-388_2257-363delinsTTGGCATTTATCCTTCCAGGCCTTTC NP_001304113.1:n.2257-388_2257-363delinsTTGGCATTTATCCTTCCAGGC...
NM_001317185.2:c.892-388_892-363delinsTTGGCATTTATCCTTCCAGGCCTTTC NP_001304114.1:n.892-388_892-363delinsTTGGCATTTATCCTTCCAGGCCT...
NM_001317186.2:c.475-388_475-363delinsTTGGCATTTATCCTTCCAGGCCTTTC NP_001304115.1:n.475-388_475-363delinsTTGGCATTTATCCTTCCAGGCCT...