Canonical Allele Identifier: CA2521001070
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737304A>G , CM000678.2:g.68737304A>G GRCh38
NC_000016.9:g.68771207A>G , CM000678.1:g.68771207A>G GRCh37
NC_000016.8:g.67328708A>G NCBI36
NG_008021.1:g.5013A>G , LRG_301:g.5013A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-112A>G MANE Select ENSP00000261769.4:n.-112A>G
ENST00000261769.9:c.-112A>G ENSP00000261769.4:n.-112A>G
ENST00000611625.4:c.-112A>G ENSP00000481063.1:n.-112A>G
ENST00000612417.4:c.-112A>G ENSP00000478360.1:n.-112A>G
NM_004360.3:c.-112A>G , LRG_301t1:c.-112A>G NP_004351.1:n.-112A>G
NM_001317184.1:c.-112A>G NP_001304113.1:n.-112A>G
NM_001317185.1:c.-1727A>G NP_001304114.1:n.-1727A>G
NM_001317186.1:c.-1931A>G NP_001304115.1:n.-1931A>G
NM_004360.4:c.-112A>G NP_004351.1:n.-112A>G
NM_004360.5:c.-112A>G MANE Select NP_004351.1:n.-112A>G
NM_001317184.2:c.-112A>G NP_001304113.1:n.-112A>G
NM_001317185.2:c.-1727A>G NP_001304114.1:n.-1727A>G
NM_001317186.2:c.-1931A>G NP_001304115.1:n.-1931A>G