Canonical Allele Identifier: CA2229980776
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822157C= , CM000678.2:g.68822157C= GRCh38
NC_000016.9:g.68856060C= , CM000678.1:g.68856060C= GRCh37
NC_000016.8:g.67413561C= NCBI36
NG_008021.1:g.89866C= , LRG_301:g.89866C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1868C= MANE Select ENSP00000261769.4:p.Thr623=
ENST00000261769.9:c.1868C= ENSP00000261769.4:p.Thr623=
ENST00000422392.6:c.1685C= ENSP00000414946.2:p.Thr562=
ENST00000562836.5:n.1939C=
ENST00000566510.5:c.*534C= ENSP00000458139.1:n.*534C=
ENST00000566612.5:c.*108C= ENSP00000454782.1:n.*108C=
ENST00000611625.4:c.1931C= ENSP00000481063.1:p.Thr644=
ENST00000612417.4:c.1830+38C= ENSP00000478360.1:n.1830+38C=
ENST00000621016.4:c.1865+3C= ENSP00000480664.1:n.1865+3C=
NM_004360.3:c.1868C= , LRG_301t1:c.1868C= NP_004351.1:p.Thr623=
XM_011523488.1:c.1133C= XP_011521790.1:p.Thr378=
XM_011523489.1:c.1133C= XP_011521791.1:p.Thr378=
NM_001317184.1:c.1685C= NP_001304113.1:p.Thr562=
NM_001317185.1:c.320C= NP_001304114.1:p.Thr107=
NM_001317186.1:c.-98C= NP_001304115.1:n.-98C=
NM_004360.4:c.1868C= NP_004351.1:p.Thr623=
NM_004360.5:c.1868C= MANE Select NP_004351.1:p.Thr623=
NM_001317184.2:c.1685C= NP_001304113.1:p.Thr562=
NM_001317185.2:c.320C= NP_001304114.1:p.Thr107=
NM_001317186.2:c.-98C= NP_001304115.1:n.-98C=