Canonical Allele Identifier: CA2229967240
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810322C= , CM000678.2:g.68810322C= GRCh38
NC_000016.9:g.68844225C= , CM000678.1:g.68844225C= GRCh37
NC_000016.8:g.67401726C= NCBI36
NG_008021.1:g.78031C= , LRG_301:g.78031C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.813C= MANE Select ENSP00000261769.4:p.Val271=
ENST00000261769.9:c.813C= ENSP00000261769.4:p.Val271=
ENST00000422392.6:c.813C= ENSP00000414946.2:p.Val271=
ENST00000561751.1:c.455-1362C=
ENST00000562836.5:n.884C=
ENST00000566510.5:c.657C= ENSP00000458139.1:p.Val219=
ENST00000566612.5:c.813C= ENSP00000454782.1:p.Val271=
ENST00000611625.4:c.813C= ENSP00000481063.1:p.Val271=
ENST00000612417.4:c.813C= ENSP00000478360.1:p.Val271=
ENST00000621016.4:c.813C= ENSP00000480664.1:p.Val271=
NM_004360.3:c.813C= , LRG_301t1:c.813C= NP_004351.1:p.Val271=
XM_011523488.1:c.78C= XP_011521790.1:p.Val26=
XM_011523489.1:c.78C= XP_011521791.1:p.Val26=
NM_001317184.1:c.813C= NP_001304113.1:p.Val271=
NM_001317185.1:c.-803C= NP_001304114.1:n.-803C=
NM_001317186.1:c.-1007C= NP_001304115.1:n.-1007C=
NM_004360.4:c.813C= NP_004351.1:p.Val271=
NM_004360.5:c.813C= MANE Select NP_004351.1:p.Val271=
NM_001317184.2:c.813C= NP_001304113.1:p.Val271=
NM_001317185.2:c.-803C= NP_001304114.1:n.-803C=
NM_001317186.2:c.-1007C= NP_001304115.1:n.-1007C=