Canonical Allele Identifier: CA2229980273
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822019G= , CM000678.2:g.68822019G= GRCh38
NC_000016.9:g.68855922G= , CM000678.1:g.68855922G= GRCh37
NC_000016.8:g.67413423G= NCBI36
NG_008021.1:g.89728G= , LRG_301:g.89728G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1730G= MANE Select ENSP00000261769.4:p.Gly577=
ENST00000261769.9:c.1730G= ENSP00000261769.4:p.Gly577=
ENST00000422392.6:c.1547G= ENSP00000414946.2:p.Gly516=
ENST00000562836.5:n.1801G=
ENST00000566510.5:c.*396G= ENSP00000458139.1:n.*396G=
ENST00000566612.5:c.1584G= ENSP00000454782.1:p.Trp528=
ENST00000611625.4:c.1793G= ENSP00000481063.1:p.Gly598=
ENST00000612417.4:c.1730G= ENSP00000478360.1:p.Gly577=
ENST00000621016.4:c.1730G= ENSP00000480664.1:p.Gly577=
NM_004360.3:c.1730G= , LRG_301t1:c.1730G= NP_004351.1:p.Gly577=
XM_011523488.1:c.995G= XP_011521790.1:p.Gly332=
XM_011523489.1:c.995G= XP_011521791.1:p.Gly332=
NM_001317184.1:c.1547G= NP_001304113.1:p.Gly516=
NM_001317185.1:c.182G= NP_001304114.1:p.Gly61=
NM_001317186.1:c.-236G= NP_001304115.1:n.-236G=
NM_004360.4:c.1730G= NP_004351.1:p.Gly577=
NM_004360.5:c.1730G= MANE Select NP_004351.1:p.Gly577=
NM_001317184.2:c.1547G= NP_001304113.1:p.Gly516=
NM_001317185.2:c.182G= NP_001304114.1:p.Gly61=
NM_001317186.2:c.-236G= NP_001304115.1:n.-236G=