Canonical Allele Identifier: CA2229978164
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833345T= , CM000678.2:g.68833345T= GRCh38
NC_000016.9:g.68867248T= , CM000678.1:g.68867248T= GRCh37
NC_000016.8:g.67424749T= NCBI36
NG_008021.1:g.101054T= , LRG_301:g.101054T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2495T= MANE Select ENSP00000261769.4:p.Val832=
ENST00000261769.9:c.2495T= ENSP00000261769.4:p.Val832=
ENST00000422392.6:c.2312T= ENSP00000414946.2:p.Val771=
ENST00000562118.1:n.713T=
ENST00000562836.5:n.2566T=
ENST00000566510.5:c.*1161T= ENSP00000458139.1:n.*1161T=
ENST00000566612.5:c.*735T= ENSP00000454782.1:n.*735T=
ENST00000611625.4:c.2558T= ENSP00000481063.1:p.Val853=
ENST00000612417.4:c.1854-846T= ENSP00000478360.1:n.1854-846T=
ENST00000621016.4:c.1866-858T= ENSP00000480664.1:n.1866-858T=
NM_004360.3:c.2495T= , LRG_301t1:c.2495T= NP_004351.1:p.Val832=
XM_011523488.1:c.1760T= XP_011521790.1:p.Val587=
XM_011523489.1:c.1760T= XP_011521791.1:p.Val587=
NM_001317184.1:c.2312T= NP_001304113.1:p.Val771=
NM_001317185.1:c.947T= NP_001304114.1:p.Val316=
NM_001317186.1:c.530T= NP_001304115.1:p.Val177=
NM_004360.4:c.2495T= NP_004351.1:p.Val832=
NM_004360.5:c.2495T= MANE Select NP_004351.1:p.Val832=
NM_001317184.2:c.2312T= NP_001304113.1:p.Val771=
NM_001317185.2:c.947T= NP_001304114.1:p.Val316=
NM_001317186.2:c.530T= NP_001304115.1:p.Val177=