Canonical Allele Identifier: CA10580070
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 233012
ClinVar RCV Id: RCV000221785
dbSNP Id: rs876660131
MyVariant Identifiers: chr16:g.68772256G>A (hg19) chr16:g.68738353G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738353G>A , CM000678.2:g.68738353G>A GRCh38
NC_000016.9:g.68772256G>A , CM000678.1:g.68772256G>A GRCh37
NC_000016.8:g.67329757G>A NCBI36
NG_008021.1:g.6062G>A , LRG_301:g.6062G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.105G>A MANE Select ENSP00000261769.4:p.Glu35=
ENST00000261769.9:c.105G>A ENSP00000261769.4:p.Glu35=
ENST00000422392.6:c.105G>A ENSP00000414946.2:p.Glu35=
ENST00000566510.5:c.105G>A ENSP00000458139.1:p.Glu35=
ENST00000566612.5:c.105G>A ENSP00000454782.1:p.Glu35=
ENST00000611625.4:c.105G>A ENSP00000481063.1:p.Glu35=
ENST00000612417.4:c.105G>A ENSP00000478360.1:p.Glu35=
ENST00000621016.4:c.105G>A ENSP00000480664.1:p.Glu35=
NM_004360.3:c.105G>A , LRG_301t1:c.105G>A NP_004351.1:p.Glu35=
NM_001317184.1:c.105G>A NP_001304113.1:p.Glu35=
NM_001317185.1:c.-1511G>A NP_001304114.1:n.-1511G>A
NM_001317186.1:c.-1715G>A NP_001304115.1:n.-1715G>A
NM_004360.4:c.105G>A NP_004351.1:p.Glu35=
NM_004360.5:c.105G>A MANE Select NP_004351.1:p.Glu35=
NM_001317184.2:c.105G>A NP_001304113.1:p.Glu35=
NM_001317185.2:c.-1511G>A NP_001304114.1:n.-1511G>A
NM_001317186.2:c.-1715G>A NP_001304115.1:n.-1715G>A
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