Canonical Allele Identifier: CA2633931986
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829768_68829773del , CM000678.2:g.68829768_68829773del GRCh38
NC_000016.9:g.68863671_68863676del , CM000678.1:g.68863671_68863676del GRCh37
NC_000016.8:g.67421172_67421177del NCBI36
NG_008021.1:g.97477_97482del , LRG_301:g.97477_97482del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2410_2415del MANE Select ENSP00000261769.4:p.Pro804_Asp805del
ENST00000261769.9:c.2410_2415del ENSP00000261769.4:p.Pro804_Asp805del
ENST00000422392.6:c.2227_2232del ENSP00000414946.2:p.Pro743_Asp744del
ENST00000562118.1:n.628_633del
ENST00000562836.5:n.2481_2486del
ENST00000566510.5:c.*1076_*1081del ENSP00000458139.1:n.*1076_*1081del
ENST00000566612.5:c.*650_*655del ENSP00000454782.1:n.*650_*655del
ENST00000611625.4:c.2473_2478del ENSP00000481063.1:p.Pro825_Asp826del
ENST00000612417.4:c.1853+3214_1853+3219del ENSP00000478360.1:n.1853+3214_1853+3219del
ENST00000621016.4:c.1866-4435_1866-4430del ENSP00000480664.1:n.1866-4435_1866-4430del
NM_004360.3:c.2410_2415del , LRG_301t1:c.2410_2415del NP_004351.1:p.Pro804_Asp805del
XM_011523488.1:c.1675_1680del XP_011521790.1:p.Pro559_Asp560del
XM_011523489.1:c.1675_1680del XP_011521791.1:p.Pro559_Asp560del
NM_001317184.1:c.2227_2232del NP_001304113.1:p.Pro743_Asp744del
NM_001317185.1:c.862_867del NP_001304114.1:p.Pro288_Asp289del
NM_001317186.1:c.445_450del NP_001304115.1:p.Pro149_Asp150del
NM_004360.4:c.2410_2415del NP_004351.1:p.Pro804_Asp805del
NM_004360.5:c.2410_2415del MANE Select NP_004351.1:p.Pro804_Asp805del
NM_001317184.2:c.2227_2232del NP_001304113.1:p.Pro743_Asp744del
NM_001317185.2:c.862_867del NP_001304114.1:p.Pro288_Asp289del
NM_001317186.2:c.445_450del NP_001304115.1:p.Pro149_Asp150del