Canonical Allele Identifier: CA2229978427
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833439C= , CM000678.2:g.68833439C= GRCh38
NC_000016.9:g.68867342C= , CM000678.1:g.68867342C= GRCh37
NC_000016.8:g.67424843C= NCBI36
NG_008021.1:g.101148C= , LRG_301:g.101148C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2589C= MANE Select ENSP00000261769.4:p.Asn863=
ENST00000261769.9:c.2589C= ENSP00000261769.4:p.Asn863=
ENST00000422392.6:c.2406C= ENSP00000414946.2:p.Asn802=
ENST00000562118.1:n.807C=
ENST00000562836.5:n.2660C=
ENST00000566510.5:c.*1255C= ENSP00000458139.1:n.*1255C=
ENST00000566612.5:c.*829C= ENSP00000454782.1:n.*829C=
ENST00000611625.4:c.2652C= ENSP00000481063.1:p.Asn884=
ENST00000612417.4:c.1854-752C= ENSP00000478360.1:n.1854-752C=
ENST00000621016.4:c.1866-764C= ENSP00000480664.1:n.1866-764C=
NM_004360.3:c.2589C= , LRG_301t1:c.2589C= NP_004351.1:p.Asn863=
XM_011523488.1:c.1854C= XP_011521790.1:p.Asn618=
XM_011523489.1:c.1854C= XP_011521791.1:p.Asn618=
NM_001317184.1:c.2406C= NP_001304113.1:p.Asn802=
NM_001317185.1:c.1041C= NP_001304114.1:p.Asn347=
NM_001317186.1:c.624C= NP_001304115.1:p.Asn208=
NM_004360.4:c.2589C= NP_004351.1:p.Asn863=
NM_004360.5:c.2589C= MANE Select NP_004351.1:p.Asn863=
NM_001317184.2:c.2406C= NP_001304113.1:p.Asn802=
NM_001317185.2:c.1041C= NP_001304114.1:p.Asn347=
NM_001317186.2:c.624C= NP_001304115.1:p.Asn208=