Canonical Allele Identifier: CA2732906787
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152143802

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833275T>G , CM000678.2:g.68833275T>G GRCh38
NC_000016.9:g.68867178T>G , CM000678.1:g.68867178T>G GRCh37
NC_000016.8:g.67424679T>G NCBI36
NG_008021.1:g.100984T>G , LRG_301:g.100984T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.2440-15T>G MANE Select ENSP00000261769.4:n.2440-15T>G
ENST00000261769.9:c.2440-15T>G ENSP00000261769.4:n.2440-15T>G
ENST00000422392.6:c.2257-15T>G ENSP00000414946.2:n.2257-15T>G
ENST00000562118.1:n.658-15T>G
ENST00000562836.5:n.2511-15T>G
ENST00000566510.5:c.*1106-15T>G ENSP00000458139.1:n.*1106-15T>G
ENST00000566612.5:c.*680-15T>G ENSP00000454782.1:n.*680-15T>G
ENST00000611625.4:c.2503-15T>G ENSP00000481063.1:n.2503-15T>G
ENST00000612417.4:c.1854-916T>G ENSP00000478360.1:n.1854-916T>G
ENST00000621016.4:c.1866-928T>G ENSP00000480664.1:n.1866-928T>G
NM_004360.3:c.2440-15T>G , LRG_301t1:c.2440-15T>G NP_004351.1:n.2440-15T>G
XM_011523488.1:c.1705-15T>G XP_011521790.1:n.1705-15T>G
XM_011523489.1:c.1705-15T>G XP_011521791.1:n.1705-15T>G
NM_001317184.1:c.2257-15T>G NP_001304113.1:n.2257-15T>G
NM_001317185.1:c.892-15T>G NP_001304114.1:n.892-15T>G
NM_001317186.1:c.475-15T>G NP_001304115.1:n.475-15T>G
NM_004360.4:c.2440-15T>G NP_004351.1:n.2440-15T>G
NM_004360.5:c.2440-15T>G MANE Select NP_004351.1:n.2440-15T>G
NM_001317184.2:c.2257-15T>G NP_001304113.1:n.2257-15T>G
NM_001317185.2:c.892-15T>G NP_001304114.1:n.892-15T>G
NM_001317186.2:c.475-15T>G NP_001304115.1:n.475-15T>G