Canonical Allele Identifier: CA2229992080
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829678_68829679delinsAG , CM000678.2:g.68829678_68829679delinsAG GRCh38
NC_000016.9:g.68863581_68863582delinsAG , CM000678.1:g.68863581_68863582delinsAG GRCh37
NC_000016.8:g.67421082_67421083delinsAG NCBI36
NG_008021.1:g.97387_97388delinsAG , LRG_301:g.97387_97388delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2320_2321delinsAG MANE Select ENSP00000261769.4:p.Arg774=
ENST00000261769.9:c.2320_2321delinsAG ENSP00000261769.4:p.Arg774=
ENST00000422392.6:c.2137_2138delinsAG ENSP00000414946.2:p.Arg713=
ENST00000562118.1:n.538_539delinsAG
ENST00000562836.5:n.2391_2392delinsAG
ENST00000566510.5:c.*986_*987delinsAG ENSP00000458139.1:n.*986_*987delinsAG
ENST00000566612.5:c.*560_*561delinsAG ENSP00000454782.1:n.*560_*561delinsAG
ENST00000611625.4:c.2383_2384delinsAG ENSP00000481063.1:p.Arg795=
ENST00000612417.4:c.1853+3124_1853+3125delinsAG ENSP00000478360.1:n.1853+3124_1853+3125delinsAG
ENST00000621016.4:c.1866-4525_1866-4524delinsAG ENSP00000480664.1:n.1866-4525_1866-4524delinsAG
NM_004360.3:c.2320_2321delinsAG , LRG_301t1:c.2320_2321delinsAG NP_004351.1:p.Arg774=
XM_011523488.1:c.1585_1586delinsAG XP_011521790.1:p.Arg529=
XM_011523489.1:c.1585_1586delinsAG XP_011521791.1:p.Arg529=
NM_001317184.1:c.2137_2138delinsAG NP_001304113.1:p.Arg713=
NM_001317185.1:c.772_773delinsAG NP_001304114.1:p.Arg258=
NM_001317186.1:c.355_356delinsAG NP_001304115.1:p.Arg119=
NM_004360.4:c.2320_2321delinsAG NP_004351.1:p.Arg774=
NM_004360.5:c.2320_2321delinsAG MANE Select NP_004351.1:p.Arg774=
NM_001317184.2:c.2137_2138delinsAG NP_001304113.1:p.Arg713=
NM_001317185.2:c.772_773delinsAG NP_001304114.1:p.Arg258=
NM_001317186.2:c.355_356delinsAG NP_001304115.1:p.Arg119=