Canonical Allele Identifier: CA2229966735
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810118C= , CM000678.2:g.68810118C= GRCh38
NC_000016.9:g.68844021C= , CM000678.1:g.68844021C= GRCh37
NC_000016.8:g.67401522C= NCBI36
NG_008021.1:g.77827C= , LRG_301:g.77827C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.688-79C= MANE Select ENSP00000261769.4:n.688-79C=
ENST00000261769.9:c.688-79C= ENSP00000261769.4:n.688-79C=
ENST00000422392.6:c.688-79C= ENSP00000414946.2:n.688-79C=
ENST00000561751.1:c.454+1270C=
ENST00000562836.5:n.759-79C=
ENST00000566510.5:c.532-79C= ENSP00000458139.1:n.532-79C=
ENST00000566612.5:c.688-79C= ENSP00000454782.1:n.688-79C=
ENST00000611625.4:c.688-79C= ENSP00000481063.1:n.688-79C=
ENST00000612417.4:c.688-79C= ENSP00000478360.1:n.688-79C=
ENST00000621016.4:c.688-79C= ENSP00000480664.1:n.688-79C=
NM_004360.3:c.688-79C= , LRG_301t1:c.688-79C= NP_004351.1:n.688-79C=
XM_011523488.1:c.-48-79C= XP_011521790.1:n.-48-79C=
XM_011523489.1:c.-48-79C= XP_011521791.1:n.-48-79C=
NM_001317184.1:c.688-79C= NP_001304113.1:n.688-79C=
NM_001317185.1:c.-928-79C= NP_001304114.1:n.-928-79C=
NM_001317186.1:c.-1132-79C= NP_001304115.1:n.-1132-79C=
NM_004360.4:c.688-79C= NP_004351.1:n.688-79C=
NM_004360.5:c.688-79C= MANE Select NP_004351.1:n.688-79C=
NM_001317184.2:c.688-79C= NP_001304113.1:n.688-79C=
NM_001317185.2:c.-928-79C= NP_001304114.1:n.-928-79C=
NM_001317186.2:c.-1132-79C= NP_001304115.1:n.-1132-79C=