Canonical Allele Identifier: CA2633932368
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823242_68823243insC , CM000678.2:g.68823242_68823243insC GRCh38
NC_000016.9:g.68857145_68857146insC , CM000678.1:g.68857145_68857146insC GRCh37
NC_000016.8:g.67414646_67414647insC NCBI36
NG_008021.1:g.90951_90952insC , LRG_301:g.90951_90952insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1937-157_1937-156insC MANE Select ENSP00000261769.4:n.1937-157_1937-156insC
ENST00000261769.9:c.1937-157_1937-156insC ENSP00000261769.4:n.1937-157_1937-156insC
ENST00000422392.6:c.1754-157_1754-156insC ENSP00000414946.2:n.1754-157_1754-156insC
ENST00000562836.5:n.2008-157_2008-156insC
ENST00000566510.5:c.*603-157_*603-156insC ENSP00000458139.1:n.*603-157_*603-156insC
ENST00000566612.5:c.*177-157_*177-156insC ENSP00000454782.1:n.*177-157_*177-156insC
ENST00000611625.4:c.2000-157_2000-156insC ENSP00000481063.1:n.2000-157_2000-156insC
ENST00000612417.4:c.1830+1123_1830+1124insC ENSP00000478360.1:n.1830+1123_1830+1124insC
ENST00000621016.4:c.1865+1088_1865+1089insC ENSP00000480664.1:n.1865+1088_1865+1089insC
NM_004360.3:c.1937-157_1937-156insC , LRG_301t1:c.1937-157_1937-156insC NP_004351.1:n.1937-157_1937-156insC
XM_011523488.1:c.1202-157_1202-156insC XP_011521790.1:n.1202-157_1202-156insC
XM_011523489.1:c.1202-157_1202-156insC XP_011521791.1:n.1202-157_1202-156insC
NM_001317184.1:c.1754-157_1754-156insC NP_001304113.1:n.1754-157_1754-156insC
NM_001317185.1:c.389-157_389-156insC NP_001304114.1:n.389-157_389-156insC
NM_001317186.1:c.-29-157_-29-156insC NP_001304115.1:n.-29-157_-29-156insC
NM_004360.4:c.1937-157_1937-156insC NP_004351.1:n.1937-157_1937-156insC
NM_004360.5:c.1937-157_1937-156insC MANE Select NP_004351.1:n.1937-157_1937-156insC
NM_001317184.2:c.1754-157_1754-156insC NP_001304113.1:n.1754-157_1754-156insC
NM_001317185.2:c.389-157_389-156insC NP_001304114.1:n.389-157_389-156insC
NM_001317186.2:c.-29-157_-29-156insC NP_001304115.1:n.-29-157_-29-156insC