Canonical Allele Identifier: CA396472563
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 654264
ClinVar RCV Id: RCV000810191 RCV004028691
dbSNP Id: rs1185746867
MyVariant Identifiers: chr16:g.68867334T>G (hg19) chr16:g.68833431T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833431T>G , CM000678.2:g.68833431T>G GRCh38
NC_000016.9:g.68867334T>G , CM000678.1:g.68867334T>G GRCh37
NC_000016.8:g.67424835T>G NCBI36
NG_008021.1:g.101140T>G , LRG_301:g.101140T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2581T>G MANE Select ENSP00000261769.4:p.Tyr861Asp
ENST00000261769.9:c.2581T>G ENSP00000261769.4:p.Tyr861Asp
ENST00000422392.6:c.2398T>G ENSP00000414946.2:p.Tyr800Asp
ENST00000562118.1:n.799T>G
ENST00000562836.5:n.2652T>G
ENST00000566510.5:c.*1247T>G ENSP00000458139.1:n.*1247T>G
ENST00000566612.5:c.*821T>G ENSP00000454782.1:n.*821T>G
ENST00000611625.4:c.2644T>G ENSP00000481063.1:p.Tyr882Asp
ENST00000612417.4:c.1854-760T>G ENSP00000478360.1:n.1854-760T>G
ENST00000621016.4:c.1866-772T>G ENSP00000480664.1:n.1866-772T>G
NM_004360.3:c.2581T>G , LRG_301t1:c.2581T>G NP_004351.1:p.Tyr861Asp
XM_011523488.1:c.1846T>G XP_011521790.1:p.Tyr616Asp
XM_011523489.1:c.1846T>G XP_011521791.1:p.Tyr616Asp
NM_001317184.1:c.2398T>G NP_001304113.1:p.Tyr800Asp
NM_001317185.1:c.1033T>G NP_001304114.1:p.Tyr345Asp
NM_001317186.1:c.616T>G NP_001304115.1:p.Tyr206Asp
NM_004360.4:c.2581T>G NP_004351.1:p.Tyr861Asp
NM_004360.5:c.2581T>G MANE Select NP_004351.1:p.Tyr861Asp
NM_001317184.2:c.2398T>G NP_001304113.1:p.Tyr800Asp
NM_001317185.2:c.1033T>G NP_001304114.1:p.Tyr345Asp
NM_001317186.2:c.616T>G NP_001304115.1:p.Tyr206Asp
Search 100 bp 5'
Search 100 bp 3'