Canonical Allele Identifier: CA2633898181
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3076087
ClinVar RCV Id: RCV004018404
dbSNP Id: rs2152113935
gnomAD v4: 16-68737409-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737409G>A , CM000678.2:g.68737409G>A GRCh38
NC_000016.9:g.68771312G>A , CM000678.1:g.68771312G>A GRCh37
NC_000016.8:g.67328813G>A NCBI36
NG_008021.1:g.5118G>A , LRG_301:g.5118G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-7G>A MANE Select ENSP00000261769.4:n.-7G>A
ENST00000261769.9:c.-7G>A ENSP00000261769.4:n.-7G>A
ENST00000422392.6:c.-7G>A ENSP00000414946.2:n.-7G>A
ENST00000566510.5:c.-7G>A ENSP00000458139.1:n.-7G>A
ENST00000566612.5:c.-7G>A ENSP00000454782.1:n.-7G>A
ENST00000611625.4:c.-7G>A ENSP00000481063.1:n.-7G>A
ENST00000612417.4:c.-7G>A ENSP00000478360.1:n.-7G>A
ENST00000621016.4:c.-7G>A ENSP00000480664.1:n.-7G>A
NM_004360.3:c.-7G>A , LRG_301t1:c.-7G>A NP_004351.1:n.-7G>A
NM_001317184.1:c.-7G>A NP_001304113.1:n.-7G>A
NM_001317185.1:c.-1622G>A NP_001304114.1:n.-1622G>A
NM_001317186.1:c.-1826G>A NP_001304115.1:n.-1826G>A
NM_004360.4:c.-7G>A NP_004351.1:n.-7G>A
NM_004360.5:c.-7G>A MANE Select NP_004351.1:n.-7G>A
NM_001317184.2:c.-7G>A NP_001304113.1:n.-7G>A
NM_001317185.2:c.-1622G>A NP_001304114.1:n.-1622G>A
NM_001317186.2:c.-1826G>A NP_001304115.1:n.-1826G>A
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