Canonical Allele Identifier: CA2229980578
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822095C= , CM000678.2:g.68822095C= GRCh38
NC_000016.9:g.68855998C= , CM000678.1:g.68855998C= GRCh37
NC_000016.8:g.67413499C= NCBI36
NG_008021.1:g.89804C= , LRG_301:g.89804C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1806C= MANE Select ENSP00000261769.4:p.Phe602=
ENST00000261769.9:c.1806C= ENSP00000261769.4:p.Phe602=
ENST00000422392.6:c.1623C= ENSP00000414946.2:p.Phe541=
ENST00000562836.5:n.1877C=
ENST00000566510.5:c.*472C= ENSP00000458139.1:n.*472C=
ENST00000566612.5:c.*46C= ENSP00000454782.1:n.*46C=
ENST00000611625.4:c.1869C= ENSP00000481063.1:p.Phe623=
ENST00000612417.4:c.1806C= ENSP00000478360.1:p.Phe602=
ENST00000621016.4:c.1806C= ENSP00000480664.1:p.Phe602=
NM_004360.3:c.1806C= , LRG_301t1:c.1806C= NP_004351.1:p.Phe602=
XM_011523488.1:c.1071C= XP_011521790.1:p.Phe357=
XM_011523489.1:c.1071C= XP_011521791.1:p.Phe357=
NM_001317184.1:c.1623C= NP_001304113.1:p.Phe541=
NM_001317185.1:c.258C= NP_001304114.1:p.Phe86=
NM_001317186.1:c.-160C= NP_001304115.1:n.-160C=
NM_004360.4:c.1806C= NP_004351.1:p.Phe602=
NM_004360.5:c.1806C= MANE Select NP_004351.1:p.Phe602=
NM_001317184.2:c.1623C= NP_001304113.1:p.Phe541=
NM_001317185.2:c.258C= NP_001304114.1:p.Phe86=
NM_001317186.2:c.-160C= NP_001304115.1:n.-160C=