Canonical Allele Identifier: CA723137215
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1341431962
MyVariant Identifiers: chr16:g.68853541del (hg19) chr16:g.68819638del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819640del , CM000678.2:g.68819640del GRCh38
NC_000016.9:g.68853543del , CM000678.1:g.68853543del GRCh37
NC_000016.8:g.67411044del NCBI36
NG_008021.1:g.87349del , LRG_301:g.87349del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1711+215del MANE Select ENSP00000261769.4:n.1711+215del
ENST00000261769.9:c.1711+215del ENSP00000261769.4:n.1711+215del
ENST00000422392.6:c.1528+215del ENSP00000414946.2:n.1528+215del
ENST00000562836.5:n.1782+215del
ENST00000566510.5:c.*377+215del ENSP00000458139.1:n.*377+215del
ENST00000566612.5:c.1566-2361del ENSP00000454782.1:n.1566-2361del
ENST00000611625.4:c.1774+215del ENSP00000481063.1:n.1774+215del
ENST00000612417.4:c.1711+215del ENSP00000478360.1:n.1711+215del
ENST00000621016.4:c.1711+215del ENSP00000480664.1:n.1711+215del
NM_004360.3:c.1711+215del , LRG_301t1:c.1711+215del NP_004351.1:n.1711+215del
XM_011523488.1:c.976+215del XP_011521790.1:n.976+215del
XM_011523489.1:c.976+215del XP_011521791.1:n.976+215del
NM_001317184.1:c.1528+215del NP_001304113.1:n.1528+215del
NM_001317185.1:c.163+215del NP_001304114.1:n.163+215del
NM_001317186.1:c.-254-2361del NP_001304115.1:n.-254-2361del
NM_004360.4:c.1711+215del NP_004351.1:n.1711+215del
NM_004360.5:c.1711+215del MANE Select NP_004351.1:n.1711+215del
NM_001317184.2:c.1528+215del NP_001304113.1:n.1528+215del
NM_001317185.2:c.163+215del NP_001304114.1:n.163+215del
NM_001317186.2:c.-254-2361del NP_001304115.1:n.-254-2361del
Search 100 bp 5'
Search 100 bp 3'