Canonical Allele Identifier: CA2229975280
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829797A= , CM000678.2:g.68829797A= GRCh38
NC_000016.9:g.68863700A= , CM000678.1:g.68863700A= GRCh37
NC_000016.8:g.67421201A= NCBI36
NG_008021.1:g.97506A= , LRG_301:g.97506A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439A= MANE Select ENSP00000261769.4:p.Glu813=
ENST00000261769.9:c.2439A= ENSP00000261769.4:p.Glu813=
ENST00000422392.6:c.2256A= ENSP00000414946.2:p.Glu752=
ENST00000562118.1:n.657A=
ENST00000562836.5:n.2510A=
ENST00000566510.5:c.*1105A= ENSP00000458139.1:n.*1105A=
ENST00000566612.5:c.*679A= ENSP00000454782.1:n.*679A=
ENST00000611625.4:c.2502A= ENSP00000481063.1:p.Glu834=
ENST00000612417.4:c.1853+3243A= ENSP00000478360.1:n.1853+3243A=
ENST00000621016.4:c.1866-4406A= ENSP00000480664.1:n.1866-4406A=
NM_004360.3:c.2439A= , LRG_301t1:c.2439A= NP_004351.1:p.Glu813=
XM_011523488.1:c.1704A= XP_011521790.1:p.Glu568=
XM_011523489.1:c.1704A= XP_011521791.1:p.Glu568=
NM_001317184.1:c.2256A= NP_001304113.1:p.Glu752=
NM_001317185.1:c.891A= NP_001304114.1:p.Glu297=
NM_001317186.1:c.474A= NP_001304115.1:p.Glu158=
NM_004360.4:c.2439A= NP_004351.1:p.Glu813=
NM_004360.5:c.2439A= MANE Select NP_004351.1:p.Glu813=
NM_001317184.2:c.2256A= NP_001304113.1:p.Glu752=
NM_001317185.2:c.891A= NP_001304114.1:p.Glu297=
NM_001317186.2:c.474A= NP_001304115.1:p.Glu158=