Canonical Allele Identifier: CA2633897211
Gene: CDH1 HGNC NCBI

Linked Data

gnomAD v4: 16-68737305-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737305C>A , CM000678.2:g.68737305C>A GRCh38
NC_000016.9:g.68771208C>A , CM000678.1:g.68771208C>A GRCh37
NC_000016.8:g.67328709C>A NCBI36
NG_008021.1:g.5014C>A , LRG_301:g.5014C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-111C>A MANE Select ENSP00000261769.4:n.-111C>A
ENST00000261769.9:c.-111C>A ENSP00000261769.4:n.-111C>A
ENST00000611625.4:c.-111C>A ENSP00000481063.1:n.-111C>A
ENST00000612417.4:c.-111C>A ENSP00000478360.1:n.-111C>A
NM_004360.3:c.-111C>A , LRG_301t1:c.-111C>A NP_004351.1:n.-111C>A
NM_001317184.1:c.-111C>A NP_001304113.1:n.-111C>A
NM_001317185.1:c.-1726C>A NP_001304114.1:n.-1726C>A
NM_001317186.1:c.-1930C>A NP_001304115.1:n.-1930C>A
NM_004360.4:c.-111C>A NP_004351.1:n.-111C>A
NM_004360.5:c.-111C>A MANE Select NP_004351.1:n.-111C>A
NM_001317184.2:c.-111C>A NP_001304113.1:n.-111C>A
NM_001317185.2:c.-1726C>A NP_001304114.1:n.-1726C>A
NM_001317186.2:c.-1930C>A NP_001304115.1:n.-1930C>A
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