Canonical Allele Identifier: CA2229966888
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810209G= , CM000678.2:g.68810209G= GRCh38
NC_000016.9:g.68844112G= , CM000678.1:g.68844112G= GRCh37
NC_000016.8:g.67401613G= NCBI36
NG_008021.1:g.77918G= , LRG_301:g.77918G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.700G= MANE Select ENSP00000261769.4:p.Ala234=
ENST00000261769.9:c.700G= ENSP00000261769.4:p.Ala234=
ENST00000422392.6:c.700G= ENSP00000414946.2:p.Ala234=
ENST00000561751.1:c.454+1361G=
ENST00000562836.5:n.771G=
ENST00000566510.5:c.544G= ENSP00000458139.1:p.Ala182=
ENST00000566612.5:c.700G= ENSP00000454782.1:p.Ala234=
ENST00000611625.4:c.700G= ENSP00000481063.1:p.Ala234=
ENST00000612417.4:c.700G= ENSP00000478360.1:p.Ala234=
ENST00000621016.4:c.700G= ENSP00000480664.1:p.Ala234=
NM_004360.3:c.700G= , LRG_301t1:c.700G= NP_004351.1:p.Ala234=
XM_011523488.1:c.-36G= XP_011521790.1:n.-36G=
XM_011523489.1:c.-36G= XP_011521791.1:n.-36G=
NM_001317184.1:c.700G= NP_001304113.1:p.Ala234=
NM_001317185.1:c.-916G= NP_001304114.1:n.-916G=
NM_001317186.1:c.-1120G= NP_001304115.1:n.-1120G=
NM_004360.4:c.700G= NP_004351.1:p.Ala234=
NM_004360.5:c.700G= MANE Select NP_004351.1:p.Ala234=
NM_001317184.2:c.700G= NP_001304113.1:p.Ala234=
NM_001317185.2:c.-916G= NP_001304114.1:n.-916G=
NM_001317186.2:c.-1120G= NP_001304115.1:n.-1120G=