Canonical Allele Identifier: CA2229967254
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810328A= , CM000678.2:g.68810328A= GRCh38
NC_000016.9:g.68844231A= , CM000678.1:g.68844231A= GRCh37
NC_000016.8:g.67401732A= NCBI36
NG_008021.1:g.78037A= , LRG_301:g.78037A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.819A= MANE Select ENSP00000261769.4:p.Glu273=
ENST00000261769.9:c.819A= ENSP00000261769.4:p.Glu273=
ENST00000422392.6:c.819A= ENSP00000414946.2:p.Glu273=
ENST00000561751.1:c.455-1356A=
ENST00000562836.5:n.890A=
ENST00000566510.5:c.663A= ENSP00000458139.1:p.Glu221=
ENST00000566612.5:c.819A= ENSP00000454782.1:p.Glu273=
ENST00000611625.4:c.819A= ENSP00000481063.1:p.Glu273=
ENST00000612417.4:c.819A= ENSP00000478360.1:p.Glu273=
ENST00000621016.4:c.819A= ENSP00000480664.1:p.Glu273=
NM_004360.3:c.819A= , LRG_301t1:c.819A= NP_004351.1:p.Glu273=
XM_011523488.1:c.84A= XP_011521790.1:p.Glu28=
XM_011523489.1:c.84A= XP_011521791.1:p.Glu28=
NM_001317184.1:c.819A= NP_001304113.1:p.Glu273=
NM_001317185.1:c.-797A= NP_001304114.1:n.-797A=
NM_001317186.1:c.-1001A= NP_001304115.1:n.-1001A=
NM_004360.4:c.819A= NP_004351.1:p.Glu273=
NM_004360.5:c.819A= MANE Select NP_004351.1:p.Glu273=
NM_001317184.2:c.819A= NP_001304113.1:p.Glu273=
NM_001317185.2:c.-797A= NP_001304114.1:n.-797A=
NM_001317186.2:c.-1001A= NP_001304115.1:n.-1001A=