Canonical Allele Identifier: CA16620249
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 421639
ClinVar RCV Id: RCV000481625 RCV000639225 RCV002402405
dbSNP Id: rs1064795267
MyVariant Identifiers: chr16:g.68849663del (hg19) chr16:g.68815760del (hg38)
ERepo: CA16620249/MONDO:0007648/007 CA16620249/MONDO:0100488/007
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68815760del , CM000678.2:g.68815760del GRCh38
NC_000016.9:g.68849663del , CM000678.1:g.68849663del GRCh37
NC_000016.8:g.67407164del NCBI36
NG_008021.1:g.83469del , LRG_301:g.83469del

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1565+1del MANE Select ENSP00000261769.4:n.1565+1del
ENST00000261769.9:c.1565+1del ENSP00000261769.4:n.1565+1del
ENST00000422392.6:c.1382+1del ENSP00000414946.2:n.1382+1del
ENST00000562836.5:n.1636+1del
ENST00000566510.5:c.*231+1del ENSP00000458139.1:n.*231+1del
ENST00000566612.5:c.1565+1del ENSP00000454782.1:n.1565+1del
ENST00000611625.4:c.1628+1del ENSP00000481063.1:n.1628+1del
ENST00000612417.4:c.1565+1del ENSP00000478360.1:n.1565+1del
ENST00000621016.4:c.1565+1del ENSP00000480664.1:n.1565+1del
NM_004360.3:c.1565+1del , LRG_301t1:c.1565+1del NP_004351.1:n.1565+1del
XM_011523488.1:c.830+1del XP_011521790.1:n.830+1del
XM_011523489.1:c.830+1del XP_011521791.1:n.830+1del
NM_001317184.1:c.1382+1del NP_001304113.1:n.1382+1del
NM_001317185.1:c.17+1del NP_001304114.1:n.17+1del
NM_001317186.1:c.-255+1del NP_001304115.1:n.-255+1del
NM_004360.4:c.1565+1del NP_004351.1:n.1565+1del
NM_004360.5:c.1565+1del MANE Select NP_004351.1:n.1565+1del
NM_001317184.2:c.1382+1del NP_001304113.1:n.1382+1del
NM_001317185.2:c.17+1del NP_001304114.1:n.17+1del
NM_001317186.2:c.-255+1del NP_001304115.1:n.-255+1del
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Search 100 bp 3'