Canonical Allele Identifier: CA2229978001
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833155_68833172delinsTTGGTGTTCACTGCTCCG , CM000678.2:g.68833155_68833172delinsTTGGTGTTCACTGCTCCG GRCh38
NC_000016.9:g.68867058_68867075delinsTTGGTGTTCACTGCTCCG , CM000678.1:g.68867058_68867075delinsTTGGTGTTCACTGCTCCG GRCh37
NC_000016.8:g.67424559_67424576delinsTTGGTGTTCACTGCTCCG NCBI36
NG_008021.1:g.100864_100881delinsTTGGTGTTCACTGCTCCG , LRG_301:g.100864_100881delinsTTGGTGTTCACTGCTCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2440-135_2440-118delinsTTGGTGTTCACTGCTCCG MANE Select ENSP00000261769.4:n.2440-135_2440-118delinsTTGGTGTTCACTGCTCCG...
ENST00000261769.9:c.2440-135_2440-118delinsTTGGTGTTCACTGCTCCG ENSP00000261769.4:n.2440-135_2440-118delinsTTGGTGTTCACTGCTCCG...
ENST00000422392.6:c.2257-135_2257-118delinsTTGGTGTTCACTGCTCCG ENSP00000414946.2:n.2257-135_2257-118delinsTTGGTGTTCACTGCTCCG...
ENST00000562118.1:n.658-135_658-118delinsTTGGTGTTCACTGCTCCG
ENST00000562836.5:n.2511-135_2511-118delinsTTGGTGTTCACTGCTCCG
ENST00000566510.5:c.*1106-135_*1106-118delinsTTGGTGTTCACTGCTCCG ENSP00000458139.1:n.*1106-135_*1106-118delinsTTGGTGTTCACTGCTC...
ENST00000566612.5:c.*680-135_*680-118delinsTTGGTGTTCACTGCTCCG ENSP00000454782.1:n.*680-135_*680-118delinsTTGGTGTTCACTGCTCCG...
ENST00000611625.4:c.2503-135_2503-118delinsTTGGTGTTCACTGCTCCG ENSP00000481063.1:n.2503-135_2503-118delinsTTGGTGTTCACTGCTCCG...
ENST00000612417.4:c.1854-1036_1854-1019delinsTTGGTGTTCACTGCTCCG ENSP00000478360.1:n.1854-1036_1854-1019delinsTTGGTGTTCACTGCTC...
ENST00000621016.4:c.1866-1048_1866-1031delinsTTGGTGTTCACTGCTCCG ENSP00000480664.1:n.1866-1048_1866-1031delinsTTGGTGTTCACTGCTC...
NM_004360.3:c.2440-135_2440-118delinsTTGGTGTTCACTGCTCCG , LRG_301t1:c.2440-135_2440-118delinsTTGGTGTTCACTGCTCCG NP_004351.1:n.2440-135_2440-118delinsTTGGTGTTCACTGCTCCG
XM_011523488.1:c.1705-135_1705-118delinsTTGGTGTTCACTGCTCCG XP_011521790.1:n.1705-135_1705-118delinsTTGGTGTTCACTGCTCCG
XM_011523489.1:c.1705-135_1705-118delinsTTGGTGTTCACTGCTCCG XP_011521791.1:n.1705-135_1705-118delinsTTGGTGTTCACTGCTCCG
NM_001317184.1:c.2257-135_2257-118delinsTTGGTGTTCACTGCTCCG NP_001304113.1:n.2257-135_2257-118delinsTTGGTGTTCACTGCTCCG
NM_001317185.1:c.892-135_892-118delinsTTGGTGTTCACTGCTCCG NP_001304114.1:n.892-135_892-118delinsTTGGTGTTCACTGCTCCG
NM_001317186.1:c.475-135_475-118delinsTTGGTGTTCACTGCTCCG NP_001304115.1:n.475-135_475-118delinsTTGGTGTTCACTGCTCCG
NM_004360.4:c.2440-135_2440-118delinsTTGGTGTTCACTGCTCCG NP_004351.1:n.2440-135_2440-118delinsTTGGTGTTCACTGCTCCG
NM_004360.5:c.2440-135_2440-118delinsTTGGTGTTCACTGCTCCG MANE Select NP_004351.1:n.2440-135_2440-118delinsTTGGTGTTCACTGCTCCG
NM_001317184.2:c.2257-135_2257-118delinsTTGGTGTTCACTGCTCCG NP_001304113.1:n.2257-135_2257-118delinsTTGGTGTTCACTGCTCCG
NM_001317185.2:c.892-135_892-118delinsTTGGTGTTCACTGCTCCG NP_001304114.1:n.892-135_892-118delinsTTGGTGTTCACTGCTCCG
NM_001317186.2:c.475-135_475-118delinsTTGGTGTTCACTGCTCCG NP_001304115.1:n.475-135_475-118delinsTTGGTGTTCACTGCTCCG