Canonical Allele Identifier: CA2229982849
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823464A= , CM000678.2:g.68823464A= GRCh38
NC_000016.9:g.68857367A= , CM000678.1:g.68857367A= GRCh37
NC_000016.8:g.67414868A= NCBI36
NG_008021.1:g.91173A= , LRG_301:g.91173A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.2002A= MANE Select ENSP00000261769.4:p.Lys668=
ENST00000261769.9:c.2002A= ENSP00000261769.4:p.Lys668=
ENST00000422392.6:c.1819A= ENSP00000414946.2:p.Lys607=
ENST00000562118.1:n.220A=
ENST00000562836.5:n.2073A=
ENST00000566510.5:c.*668A= ENSP00000458139.1:n.*668A=
ENST00000566612.5:c.*242A= ENSP00000454782.1:n.*242A=
ENST00000611625.4:c.2065A= ENSP00000481063.1:p.Lys689=
ENST00000612417.4:c.1830+1345A= ENSP00000478360.1:n.1830+1345A=
ENST00000621016.4:c.1865+1310A= ENSP00000480664.1:n.1865+1310A=
NM_004360.3:c.2002A= , LRG_301t1:c.2002A= NP_004351.1:p.Lys668=
XM_011523488.1:c.1267A= XP_011521790.1:p.Lys423=
XM_011523489.1:c.1267A= XP_011521791.1:p.Lys423=
NM_001317184.1:c.1819A= NP_001304113.1:p.Lys607=
NM_001317185.1:c.454A= NP_001304114.1:p.Lys152=
NM_001317186.1:c.37A= NP_001304115.1:p.Lys13=
NM_004360.4:c.2002A= NP_004351.1:p.Lys668=
NM_004360.5:c.2002A= MANE Select NP_004351.1:p.Lys668=
NM_001317184.2:c.1819A= NP_001304113.1:p.Lys607=
NM_001317185.2:c.454A= NP_001304114.1:p.Lys152=
NM_001317186.2:c.37A= NP_001304115.1:p.Lys13=