Canonical Allele Identifier: CA396471946
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833292T>A , CM000678.2:g.68833292T>A GRCh38
NC_000016.9:g.68867195T>A , CM000678.1:g.68867195T>A GRCh37
NC_000016.8:g.67424696T>A NCBI36
NG_008021.1:g.101001T>A , LRG_301:g.101001T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2442T>A MANE Select ENSP00000261769.4:p.Asn814Lys
ENST00000261769.9:c.2442T>A ENSP00000261769.4:p.Asn814Lys
ENST00000422392.6:c.2259T>A ENSP00000414946.2:p.Asn753Lys
ENST00000562118.1:n.660T>A
ENST00000562836.5:n.2513T>A
ENST00000566510.5:c.*1108T>A ENSP00000458139.1:n.*1108T>A
ENST00000566612.5:c.*682T>A ENSP00000454782.1:n.*682T>A
ENST00000611625.4:c.2505T>A ENSP00000481063.1:p.Asn835Lys
ENST00000612417.4:c.1854-899T>A ENSP00000478360.1:n.1854-899T>A
ENST00000621016.4:c.1866-911T>A ENSP00000480664.1:n.1866-911T>A
NM_004360.3:c.2442T>A , LRG_301t1:c.2442T>A NP_004351.1:p.Asn814Lys
XM_011523488.1:c.1707T>A XP_011521790.1:p.Asn569Lys
XM_011523489.1:c.1707T>A XP_011521791.1:p.Asn569Lys
NM_001317184.1:c.2259T>A NP_001304113.1:p.Asn753Lys
NM_001317185.1:c.894T>A NP_001304114.1:p.Asn298Lys
NM_001317186.1:c.477T>A NP_001304115.1:p.Asn159Lys
NM_004360.4:c.2442T>A NP_004351.1:p.Asn814Lys
NM_004360.5:c.2442T>A MANE Select NP_004351.1:p.Asn814Lys
NM_001317184.2:c.2259T>A NP_001304113.1:p.Asn753Lys
NM_001317185.2:c.894T>A NP_001304114.1:p.Asn298Lys
NM_001317186.2:c.477T>A NP_001304115.1:p.Asn159Lys