Canonical Allele Identifier: CA2229980412
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822055A= , CM000678.2:g.68822055A= GRCh38
NC_000016.9:g.68855958A= , CM000678.1:g.68855958A= GRCh37
NC_000016.8:g.67413459A= NCBI36
NG_008021.1:g.89764A= , LRG_301:g.89764A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1766A= MANE Select ENSP00000261769.4:p.Asn589=
ENST00000261769.9:c.1766A= ENSP00000261769.4:p.Asn589=
ENST00000422392.6:c.1583A= ENSP00000414946.2:p.Asn528=
ENST00000562836.5:n.1837A=
ENST00000566510.5:c.*432A= ENSP00000458139.1:n.*432A=
ENST00000566612.5:c.*6A= ENSP00000454782.1:n.*6A=
ENST00000611625.4:c.1829A= ENSP00000481063.1:p.Asn610=
ENST00000612417.4:c.1766A= ENSP00000478360.1:p.Asn589=
ENST00000621016.4:c.1766A= ENSP00000480664.1:p.Asn589=
NM_004360.3:c.1766A= , LRG_301t1:c.1766A= NP_004351.1:p.Asn589=
XM_011523488.1:c.1031A= XP_011521790.1:p.Asn344=
XM_011523489.1:c.1031A= XP_011521791.1:p.Asn344=
NM_001317184.1:c.1583A= NP_001304113.1:p.Asn528=
NM_001317185.1:c.218A= NP_001304114.1:p.Asn73=
NM_001317186.1:c.-200A= NP_001304115.1:n.-200A=
NM_004360.4:c.1766A= NP_004351.1:p.Asn589=
NM_004360.5:c.1766A= MANE Select NP_004351.1:p.Asn589=
NM_001317184.2:c.1583A= NP_001304113.1:p.Asn528=
NM_001317185.2:c.218A= NP_001304114.1:p.Asn73=
NM_001317186.2:c.-200A= NP_001304115.1:n.-200A=