Canonical Allele Identifier: CA496152821
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486831
ClinVar RCV Id: RCV000573142 RCV003512055
dbSNP Id: rs1300078492
gnomAD v4: 16-68810322-C-G
MyVariant Identifiers: chr16:g.68844225C>G (hg19) chr16:g.68810322C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810322C>G , CM000678.2:g.68810322C>G GRCh38
NC_000016.9:g.68844225C>G , CM000678.1:g.68844225C>G GRCh37
NC_000016.8:g.67401726C>G NCBI36
NG_008021.1:g.78031C>G , LRG_301:g.78031C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.813C>G MANE Select ENSP00000261769.4:p.Val271=
ENST00000261769.9:c.813C>G ENSP00000261769.4:p.Val271=
ENST00000422392.6:c.813C>G ENSP00000414946.2:p.Val271=
ENST00000561751.1:c.455-1362C>G
ENST00000562836.5:n.884C>G
ENST00000566510.5:c.657C>G ENSP00000458139.1:p.Val219=
ENST00000566612.5:c.813C>G ENSP00000454782.1:p.Val271=
ENST00000611625.4:c.813C>G ENSP00000481063.1:p.Val271=
ENST00000612417.4:c.813C>G ENSP00000478360.1:p.Val271=
ENST00000621016.4:c.813C>G ENSP00000480664.1:p.Val271=
NM_004360.3:c.813C>G , LRG_301t1:c.813C>G NP_004351.1:p.Val271=
XM_011523488.1:c.78C>G XP_011521790.1:p.Val26=
XM_011523489.1:c.78C>G XP_011521791.1:p.Val26=
NM_001317184.1:c.813C>G NP_001304113.1:p.Val271=
NM_001317185.1:c.-803C>G NP_001304114.1:n.-803C>G
NM_001317186.1:c.-1007C>G NP_001304115.1:n.-1007C>G
NM_004360.4:c.813C>G NP_004351.1:p.Val271=
NM_004360.5:c.813C>G MANE Select NP_004351.1:p.Val271=
NM_001317184.2:c.813C>G NP_001304113.1:p.Val271=
NM_001317185.2:c.-803C>G NP_001304114.1:n.-803C>G
NM_001317186.2:c.-1007C>G NP_001304115.1:n.-1007C>G
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