Canonical Allele Identifier: CA2229978178
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833356G= , CM000678.2:g.68833356G= GRCh38
NC_000016.9:g.68867259G= , CM000678.1:g.68867259G= GRCh37
NC_000016.8:g.67424760G= NCBI36
NG_008021.1:g.101065G= , LRG_301:g.101065G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2506G= MANE Select ENSP00000261769.4:p.Glu836=
ENST00000261769.9:c.2506G= ENSP00000261769.4:p.Glu836=
ENST00000422392.6:c.2323G= ENSP00000414946.2:p.Glu775=
ENST00000562118.1:n.724G=
ENST00000562836.5:n.2577G=
ENST00000566510.5:c.*1172G= ENSP00000458139.1:n.*1172G=
ENST00000566612.5:c.*746G= ENSP00000454782.1:n.*746G=
ENST00000611625.4:c.2569G= ENSP00000481063.1:p.Glu857=
ENST00000612417.4:c.1854-835G= ENSP00000478360.1:n.1854-835G=
ENST00000621016.4:c.1866-847G= ENSP00000480664.1:n.1866-847G=
NM_004360.3:c.2506G= , LRG_301t1:c.2506G= NP_004351.1:p.Glu836=
XM_011523488.1:c.1771G= XP_011521790.1:p.Glu591=
XM_011523489.1:c.1771G= XP_011521791.1:p.Glu591=
NM_001317184.1:c.2323G= NP_001304113.1:p.Glu775=
NM_001317185.1:c.958G= NP_001304114.1:p.Glu320=
NM_001317186.1:c.541G= NP_001304115.1:p.Glu181=
NM_004360.4:c.2506G= NP_004351.1:p.Glu836=
NM_004360.5:c.2506G= MANE Select NP_004351.1:p.Glu836=
NM_001317184.2:c.2323G= NP_001304113.1:p.Glu775=
NM_001317185.2:c.958G= NP_001304114.1:p.Glu320=
NM_001317186.2:c.541G= NP_001304115.1:p.Glu181=