Canonical Allele Identifier: CA2229980400
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822049A= , CM000678.2:g.68822049A= GRCh38
NC_000016.9:g.68855952A= , CM000678.1:g.68855952A= GRCh37
NC_000016.8:g.67413453A= NCBI36
NG_008021.1:g.89758A= , LRG_301:g.89758A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1760A= MANE Select ENSP00000261769.4:p.Asp587=
ENST00000261769.9:c.1760A= ENSP00000261769.4:p.Asp587=
ENST00000422392.6:c.1577A= ENSP00000414946.2:p.Asp526=
ENST00000562836.5:n.1831A=
ENST00000566510.5:c.*426A= ENSP00000458139.1:n.*426A=
ENST00000566612.5:c.1614A= ENSP00000454782.1:p.Ter538=
ENST00000611625.4:c.1823A= ENSP00000481063.1:p.Asp608=
ENST00000612417.4:c.1760A= ENSP00000478360.1:p.Asp587=
ENST00000621016.4:c.1760A= ENSP00000480664.1:p.Asp587=
NM_004360.3:c.1760A= , LRG_301t1:c.1760A= NP_004351.1:p.Asp587=
XM_011523488.1:c.1025A= XP_011521790.1:p.Asp342=
XM_011523489.1:c.1025A= XP_011521791.1:p.Asp342=
NM_001317184.1:c.1577A= NP_001304113.1:p.Asp526=
NM_001317185.1:c.212A= NP_001304114.1:p.Asp71=
NM_001317186.1:c.-206A= NP_001304115.1:n.-206A=
NM_004360.4:c.1760A= NP_004351.1:p.Asp587=
NM_004360.5:c.1760A= MANE Select NP_004351.1:p.Asp587=
NM_001317184.2:c.1577A= NP_001304113.1:p.Asp526=
NM_001317185.2:c.212A= NP_001304114.1:p.Asp71=
NM_001317186.2:c.-206A= NP_001304115.1:n.-206A=