Canonical Allele Identifier: CA496393094
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68867276A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833373A>G , CM000678.2:g.68833373A>G GRCh38
NC_000016.9:g.68867276A>G , CM000678.1:g.68867276A>G GRCh37
NC_000016.8:g.67424777A>G NCBI36
NG_008021.1:g.101082A>G , LRG_301:g.101082A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2523A>G MANE Select ENSP00000261769.4:p.Glu841=
ENST00000261769.9:c.2523A>G ENSP00000261769.4:p.Glu841=
ENST00000422392.6:c.2340A>G ENSP00000414946.2:p.Glu780=
ENST00000562118.1:n.741A>G
ENST00000562836.5:n.2594A>G
ENST00000566510.5:c.*1189A>G ENSP00000458139.1:n.*1189A>G
ENST00000566612.5:c.*763A>G ENSP00000454782.1:n.*763A>G
ENST00000611625.4:c.2586A>G ENSP00000481063.1:p.Glu862=
ENST00000612417.4:c.1854-818A>G ENSP00000478360.1:n.1854-818A>G
ENST00000621016.4:c.1866-830A>G ENSP00000480664.1:n.1866-830A>G
NM_004360.3:c.2523A>G , LRG_301t1:c.2523A>G NP_004351.1:p.Glu841=
XM_011523488.1:c.1788A>G XP_011521790.1:p.Glu596=
XM_011523489.1:c.1788A>G XP_011521791.1:p.Glu596=
NM_001317184.1:c.2340A>G NP_001304113.1:p.Glu780=
NM_001317185.1:c.975A>G NP_001304114.1:p.Glu325=
NM_001317186.1:c.558A>G NP_001304115.1:p.Glu186=
NM_004360.4:c.2523A>G NP_004351.1:p.Glu841=
NM_004360.5:c.2523A>G MANE Select NP_004351.1:p.Glu841=
NM_001317184.2:c.2340A>G NP_001304113.1:p.Glu780=
NM_001317185.2:c.975A>G NP_001304114.1:p.Glu325=
NM_001317186.2:c.558A>G NP_001304115.1:p.Glu186=