Canonical Allele Identifier: CA10580161
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 231547
ClinVar RCV Id: RCV000214749 RCV000471268 RCV003462466
dbSNP Id: rs876659218
gnomAD v4: 16-68829714-G-A
MyVariant Identifiers: chr16:g.68863617G>A (hg19) chr16:g.68829714G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829714G>A , CM000678.2:g.68829714G>A GRCh38
NC_000016.9:g.68863617G>A , CM000678.1:g.68863617G>A GRCh37
NC_000016.8:g.67421118G>A NCBI36
NG_008021.1:g.97423G>A , LRG_301:g.97423G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2356G>A MANE Select ENSP00000261769.4:p.Asp786Asn
ENST00000261769.9:c.2356G>A ENSP00000261769.4:p.Asp786Asn
ENST00000422392.6:c.2173G>A ENSP00000414946.2:p.Asp725Asn
ENST00000562118.1:n.574G>A
ENST00000562836.5:n.2427G>A
ENST00000566510.5:c.*1022G>A ENSP00000458139.1:n.*1022G>A
ENST00000566612.5:c.*596G>A ENSP00000454782.1:n.*596G>A
ENST00000611625.4:c.2419G>A ENSP00000481063.1:p.Asp807Asn
ENST00000612417.4:c.1853+3160G>A ENSP00000478360.1:n.1853+3160G>A
ENST00000621016.4:c.1866-4489G>A ENSP00000480664.1:n.1866-4489G>A
NM_004360.3:c.2356G>A , LRG_301t1:c.2356G>A NP_004351.1:p.Asp786Asn
XM_011523488.1:c.1621G>A XP_011521790.1:p.Asp541Asn
XM_011523489.1:c.1621G>A XP_011521791.1:p.Asp541Asn
NM_001317184.1:c.2173G>A NP_001304113.1:p.Asp725Asn
NM_001317185.1:c.808G>A NP_001304114.1:p.Asp270Asn
NM_001317186.1:c.391G>A NP_001304115.1:p.Asp131Asn
NM_004360.4:c.2356G>A NP_004351.1:p.Asp786Asn
NM_004360.5:c.2356G>A MANE Select NP_004351.1:p.Asp786Asn
NM_001317184.2:c.2173G>A NP_001304113.1:p.Asp725Asn
NM_001317185.2:c.808G>A NP_001304114.1:p.Asp270Asn
NM_001317186.2:c.391G>A NP_001304115.1:p.Asp131Asn
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