Canonical Allele Identifier: CA2229978448
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833443T= , CM000678.2:g.68833443T= GRCh38
NC_000016.9:g.68867346T= , CM000678.1:g.68867346T= GRCh37
NC_000016.8:g.67424847T= NCBI36
NG_008021.1:g.101152T= , LRG_301:g.101152T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2593T= MANE Select ENSP00000261769.4:p.Trp865=
ENST00000261769.9:c.2593T= ENSP00000261769.4:p.Trp865=
ENST00000422392.6:c.2410T= ENSP00000414946.2:p.Trp804=
ENST00000562118.1:n.811T=
ENST00000562836.5:n.2664T=
ENST00000566510.5:c.*1259T= ENSP00000458139.1:n.*1259T=
ENST00000566612.5:c.*833T= ENSP00000454782.1:n.*833T=
ENST00000611625.4:c.2656T= ENSP00000481063.1:p.Trp886=
ENST00000612417.4:c.1854-748T= ENSP00000478360.1:n.1854-748T=
ENST00000621016.4:c.1866-760T= ENSP00000480664.1:n.1866-760T=
NM_004360.3:c.2593T= , LRG_301t1:c.2593T= NP_004351.1:p.Trp865=
XM_011523488.1:c.1858T= XP_011521790.1:p.Trp620=
XM_011523489.1:c.1858T= XP_011521791.1:p.Trp620=
NM_001317184.1:c.2410T= NP_001304113.1:p.Trp804=
NM_001317185.1:c.1045T= NP_001304114.1:p.Trp349=
NM_001317186.1:c.628T= NP_001304115.1:p.Trp210=
NM_004360.4:c.2593T= NP_004351.1:p.Trp865=
NM_004360.5:c.2593T= MANE Select NP_004351.1:p.Trp865=
NM_001317184.2:c.2410T= NP_001304113.1:p.Trp804=
NM_001317185.2:c.1045T= NP_001304114.1:p.Trp349=
NM_001317186.2:c.628T= NP_001304115.1:p.Trp210=