Canonical Allele Identifier: CA2229978182
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833360G= , CM000678.2:g.68833360G= GRCh38
NC_000016.9:g.68867263G= , CM000678.1:g.68867263G= GRCh37
NC_000016.8:g.67424764G= NCBI36
NG_008021.1:g.101069G= , LRG_301:g.101069G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2510G= MANE Select ENSP00000261769.4:p.Gly837=
ENST00000261769.9:c.2510G= ENSP00000261769.4:p.Gly837=
ENST00000422392.6:c.2327G= ENSP00000414946.2:p.Gly776=
ENST00000562118.1:n.728G=
ENST00000562836.5:n.2581G=
ENST00000566510.5:c.*1176G= ENSP00000458139.1:n.*1176G=
ENST00000566612.5:c.*750G= ENSP00000454782.1:n.*750G=
ENST00000611625.4:c.2573G= ENSP00000481063.1:p.Gly858=
ENST00000612417.4:c.1854-831G= ENSP00000478360.1:n.1854-831G=
ENST00000621016.4:c.1866-843G= ENSP00000480664.1:n.1866-843G=
NM_004360.3:c.2510G= , LRG_301t1:c.2510G= NP_004351.1:p.Gly837=
XM_011523488.1:c.1775G= XP_011521790.1:p.Gly592=
XM_011523489.1:c.1775G= XP_011521791.1:p.Gly592=
NM_001317184.1:c.2327G= NP_001304113.1:p.Gly776=
NM_001317185.1:c.962G= NP_001304114.1:p.Gly321=
NM_001317186.1:c.545G= NP_001304115.1:p.Gly182=
NM_004360.4:c.2510G= NP_004351.1:p.Gly837=
NM_004360.5:c.2510G= MANE Select NP_004351.1:p.Gly837=
NM_001317184.2:c.2327G= NP_001304113.1:p.Gly776=
NM_001317185.2:c.962G= NP_001304114.1:p.Gly321=
NM_001317186.2:c.545G= NP_001304115.1:p.Gly182=