Canonical Allele Identifier: CA2633897385
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737323C>G , CM000678.2:g.68737323C>G GRCh38
NC_000016.9:g.68771226C>G , CM000678.1:g.68771226C>G GRCh37
NC_000016.8:g.67328727C>G NCBI36
NG_008021.1:g.5032C>G , LRG_301:g.5032C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-93C>G MANE Select ENSP00000261769.4:n.-93C>G
ENST00000261769.9:c.-93C>G ENSP00000261769.4:n.-93C>G
ENST00000566612.5:c.-93C>G ENSP00000454782.1:n.-93C>G
ENST00000611625.4:c.-93C>G ENSP00000481063.1:n.-93C>G
ENST00000612417.4:c.-93C>G ENSP00000478360.1:n.-93C>G
ENST00000621016.4:c.-93C>G ENSP00000480664.1:n.-93C>G
NM_004360.3:c.-93C>G , LRG_301t1:c.-93C>G NP_004351.1:n.-93C>G
NM_001317184.1:c.-93C>G NP_001304113.1:n.-93C>G
NM_001317185.1:c.-1708C>G NP_001304114.1:n.-1708C>G
NM_001317186.1:c.-1912C>G NP_001304115.1:n.-1912C>G
NM_004360.4:c.-93C>G NP_004351.1:n.-93C>G
NM_004360.5:c.-93C>G MANE Select NP_004351.1:n.-93C>G
NM_001317184.2:c.-93C>G NP_001304113.1:n.-93C>G
NM_001317185.2:c.-1708C>G NP_001304114.1:n.-1708C>G
NM_001317186.2:c.-1912C>G NP_001304115.1:n.-1912C>G