Canonical Allele Identifier: CA10577530
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 234282
ClinVar RCV Id: RCV000220774 RCV003328293
dbSNP Id: rs876660969
gnomAD v4: 16-68737366-C-G
MyVariant Identifiers: chr16:g.68771269C>G (hg19) chr16:g.68737366C>G (hg38)
ERepo: CA10577530/MONDO:0007648/007 CA10577530/MONDO:0100488/007
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737366C>G , CM000678.2:g.68737366C>G GRCh38
NC_000016.9:g.68771269C>G , CM000678.1:g.68771269C>G GRCh37
NC_000016.8:g.67328770C>G NCBI36
NG_008021.1:g.5075C>G , LRG_301:g.5075C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-50C>G MANE Select ENSP00000261769.4:n.-50C>G
ENST00000261769.9:c.-50C>G ENSP00000261769.4:n.-50C>G
ENST00000422392.6:c.-50C>G ENSP00000414946.2:n.-50C>G
ENST00000566510.5:c.-50C>G ENSP00000458139.1:n.-50C>G
ENST00000566612.5:c.-50C>G ENSP00000454782.1:n.-50C>G
ENST00000611625.4:c.-50C>G ENSP00000481063.1:n.-50C>G
ENST00000612417.4:c.-50C>G ENSP00000478360.1:n.-50C>G
ENST00000621016.4:c.-50C>G ENSP00000480664.1:n.-50C>G
NM_004360.3:c.-50C>G , LRG_301t1:c.-50C>G NP_004351.1:n.-50C>G
NM_001317184.1:c.-50C>G NP_001304113.1:n.-50C>G
NM_001317185.1:c.-1665C>G NP_001304114.1:n.-1665C>G
NM_001317186.1:c.-1869C>G NP_001304115.1:n.-1869C>G
NM_004360.4:c.-50C>G NP_004351.1:n.-50C>G
NM_004360.5:c.-50C>G MANE Select NP_004351.1:n.-50C>G
NM_001317184.2:c.-50C>G NP_001304113.1:n.-50C>G
NM_001317185.2:c.-1665C>G NP_001304114.1:n.-1665C>G
NM_001317186.2:c.-1869C>G NP_001304115.1:n.-1869C>G
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