Canonical Allele Identifier: CA2229981008
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822205_68822207delinsCCA , CM000678.2:g.68822205_68822207delinsCCA GRCh38
NC_000016.9:g.68856108_68856110delinsCCA , CM000678.1:g.68856108_68856110delinsCCA GRCh37
NC_000016.8:g.67413609_67413611delinsCCA NCBI36
NG_008021.1:g.89914_89916delinsCCA , LRG_301:g.89914_89916delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1916_1918delinsCCA MANE Select ENSP00000261769.4:p.Thr639=
ENST00000261769.9:c.1916_1918delinsCCA ENSP00000261769.4:p.Thr639=
ENST00000422392.6:c.1733_1735delinsCCA ENSP00000414946.2:p.Thr578=
ENST00000562836.5:n.1987_1989delinsCCA
ENST00000566510.5:c.*582_*584delinsCCA ENSP00000458139.1:n.*582_*584delinsCCA
ENST00000566612.5:c.*156_*158delinsCCA ENSP00000454782.1:n.*156_*158delinsCCA
ENST00000611625.4:c.1979_1981delinsCCA ENSP00000481063.1:p.Thr660=
ENST00000612417.4:c.1830+86_1830+88delinsCCA ENSP00000478360.1:n.1830+86_1830+88delinsCCA
ENST00000621016.4:c.1865+51_1865+53delinsCCA ENSP00000480664.1:n.1865+51_1865+53delinsCCA
NM_004360.3:c.1916_1918delinsCCA , LRG_301t1:c.1916_1918delinsCCA NP_004351.1:p.Thr639=
XM_011523488.1:c.1181_1183delinsCCA XP_011521790.1:p.Thr394=
XM_011523489.1:c.1181_1183delinsCCA XP_011521791.1:p.Thr394=
NM_001317184.1:c.1733_1735delinsCCA NP_001304113.1:p.Thr578=
NM_001317185.1:c.368_370delinsCCA NP_001304114.1:p.Thr123=
NM_001317186.1:c.-50_-48delinsCCA NP_001304115.1:n.-50_-48delinsCCA
NM_004360.4:c.1916_1918delinsCCA NP_004351.1:p.Thr639=
NM_004360.5:c.1916_1918delinsCCA MANE Select NP_004351.1:p.Thr639=
NM_001317184.2:c.1733_1735delinsCCA NP_001304113.1:p.Thr578=
NM_001317185.2:c.368_370delinsCCA NP_001304114.1:p.Thr123=
NM_001317186.2:c.-50_-48delinsCCA NP_001304115.1:n.-50_-48delinsCCA