Canonical Allele Identifier: CA2633897207
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1015488305

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737303A>G , CM000678.2:g.68737303A>G GRCh38
NC_000016.9:g.68771206A>G , CM000678.1:g.68771206A>G GRCh37
NC_000016.8:g.67328707A>G NCBI36
NG_008021.1:g.5012A>G , LRG_301:g.5012A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.-113A>G MANE Select ENSP00000261769.4:n.-113A>G
ENST00000261769.9:c.-113A>G ENSP00000261769.4:n.-113A>G
ENST00000611625.4:c.-113A>G ENSP00000481063.1:n.-113A>G
ENST00000612417.4:c.-113A>G ENSP00000478360.1:n.-113A>G
NM_004360.3:c.-113A>G , LRG_301t1:c.-113A>G NP_004351.1:n.-113A>G
NM_001317184.1:c.-113A>G NP_001304113.1:n.-113A>G
NM_001317185.1:c.-1728A>G NP_001304114.1:n.-1728A>G
NM_001317186.1:c.-1932A>G NP_001304115.1:n.-1932A>G
NM_004360.4:c.-113A>G NP_004351.1:n.-113A>G
NM_004360.5:c.-113A>G MANE Select NP_004351.1:n.-113A>G
NM_001317184.2:c.-113A>G NP_001304113.1:n.-113A>G
NM_001317185.2:c.-1728A>G NP_001304114.1:n.-1728A>G
NM_001317186.2:c.-1932A>G NP_001304115.1:n.-1932A>G