Canonical Allele Identifier: CA2229983225
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823553G= , CM000678.2:g.68823553G= GRCh38
NC_000016.9:g.68857456G= , CM000678.1:g.68857456G= GRCh37
NC_000016.8:g.67414957G= NCBI36
NG_008021.1:g.91262G= , LRG_301:g.91262G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.2091G= MANE Select ENSP00000261769.4:p.Lys697=
ENST00000261769.9:c.2091G= ENSP00000261769.4:p.Lys697=
ENST00000422392.6:c.1908G= ENSP00000414946.2:p.Lys636=
ENST00000562118.1:n.309G=
ENST00000562836.5:n.2162G=
ENST00000566510.5:c.*757G= ENSP00000458139.1:n.*757G=
ENST00000566612.5:c.*331G= ENSP00000454782.1:n.*331G=
ENST00000611625.4:c.2154G= ENSP00000481063.1:p.Lys718=
ENST00000612417.4:c.1830+1434G= ENSP00000478360.1:n.1830+1434G=
ENST00000621016.4:c.1865+1399G= ENSP00000480664.1:n.1865+1399G=
NM_004360.3:c.2091G= , LRG_301t1:c.2091G= NP_004351.1:p.Lys697=
XM_011523488.1:c.1356G= XP_011521790.1:p.Lys452=
XM_011523489.1:c.1356G= XP_011521791.1:p.Lys452=
NM_001317184.1:c.1908G= NP_001304113.1:p.Lys636=
NM_001317185.1:c.543G= NP_001304114.1:p.Lys181=
NM_001317186.1:c.126G= NP_001304115.1:p.Lys42=
NM_004360.4:c.2091G= NP_004351.1:p.Lys697=
NM_004360.5:c.2091G= MANE Select NP_004351.1:p.Lys697=
NM_001317184.2:c.1908G= NP_001304113.1:p.Lys636=
NM_001317185.2:c.543G= NP_001304114.1:p.Lys181=
NM_001317186.2:c.126G= NP_001304115.1:p.Lys42=