Canonical Allele Identifier: CA2633932388
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823258_68823260del , CM000678.2:g.68823258_68823260del GRCh38
NC_000016.9:g.68857161_68857163del , CM000678.1:g.68857161_68857163del GRCh37
NC_000016.8:g.67414662_67414664del NCBI36
NG_008021.1:g.90967_90969del , LRG_301:g.90967_90969del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1937-141_1937-139del MANE Select ENSP00000261769.4:n.1937-141_1937-139del
ENST00000261769.9:c.1937-141_1937-139del ENSP00000261769.4:n.1937-141_1937-139del
ENST00000422392.6:c.1754-141_1754-139del ENSP00000414946.2:n.1754-141_1754-139del
ENST00000562118.1:n.14_16del
ENST00000562836.5:n.2008-141_2008-139del
ENST00000566510.5:c.*603-141_*603-139del ENSP00000458139.1:n.*603-141_*603-139del
ENST00000566612.5:c.*177-141_*177-139del ENSP00000454782.1:n.*177-141_*177-139del
ENST00000611625.4:c.2000-141_2000-139del ENSP00000481063.1:n.2000-141_2000-139del
ENST00000612417.4:c.1830+1139_1830+1141del ENSP00000478360.1:n.1830+1139_1830+1141del
ENST00000621016.4:c.1865+1104_1865+1106del ENSP00000480664.1:n.1865+1104_1865+1106del
NM_004360.3:c.1937-141_1937-139del , LRG_301t1:c.1937-141_1937-139del NP_004351.1:n.1937-141_1937-139del
XM_011523488.1:c.1202-141_1202-139del XP_011521790.1:n.1202-141_1202-139del
XM_011523489.1:c.1202-141_1202-139del XP_011521791.1:n.1202-141_1202-139del
NM_001317184.1:c.1754-141_1754-139del NP_001304113.1:n.1754-141_1754-139del
NM_001317185.1:c.389-141_389-139del NP_001304114.1:n.389-141_389-139del
NM_001317186.1:c.-29-141_-29-139del NP_001304115.1:n.-29-141_-29-139del
NM_004360.4:c.1937-141_1937-139del NP_004351.1:n.1937-141_1937-139del
NM_004360.5:c.1937-141_1937-139del MANE Select NP_004351.1:n.1937-141_1937-139del
NM_001317184.2:c.1754-141_1754-139del NP_001304113.1:n.1754-141_1754-139del
NM_001317185.2:c.389-141_389-139del NP_001304114.1:n.389-141_389-139del
NM_001317186.2:c.-29-141_-29-139del NP_001304115.1:n.-29-141_-29-139del