Canonical Allele Identifier: CA2732636121
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1596972979

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829832C>G , CM000678.2:g.68829832C>G GRCh38
NC_000016.9:g.68863735C>G , CM000678.1:g.68863735C>G GRCh37
NC_000016.8:g.67421236C>G NCBI36
NG_008021.1:g.97541C>G , LRG_301:g.97541C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+35C>G MANE Select ENSP00000261769.4:n.2439+35C>G
ENST00000261769.9:c.2439+35C>G ENSP00000261769.4:n.2439+35C>G
ENST00000422392.6:c.2256+35C>G ENSP00000414946.2:n.2256+35C>G
ENST00000562118.1:n.657+35C>G
ENST00000562836.5:n.2510+35C>G
ENST00000566510.5:c.*1105+35C>G ENSP00000458139.1:n.*1105+35C>G
ENST00000566612.5:c.*679+35C>G ENSP00000454782.1:n.*679+35C>G
ENST00000611625.4:c.2502+35C>G ENSP00000481063.1:n.2502+35C>G
ENST00000612417.4:c.1853+3278C>G ENSP00000478360.1:n.1853+3278C>G
ENST00000621016.4:c.1866-4371C>G ENSP00000480664.1:n.1866-4371C>G
NM_004360.3:c.2439+35C>G , LRG_301t1:c.2439+35C>G NP_004351.1:n.2439+35C>G
XM_011523488.1:c.1704+35C>G XP_011521790.1:n.1704+35C>G
XM_011523489.1:c.1704+35C>G XP_011521791.1:n.1704+35C>G
NM_001317184.1:c.2256+35C>G NP_001304113.1:n.2256+35C>G
NM_001317185.1:c.891+35C>G NP_001304114.1:n.891+35C>G
NM_001317186.1:c.474+35C>G NP_001304115.1:n.474+35C>G
NM_004360.4:c.2439+35C>G NP_004351.1:n.2439+35C>G
NM_004360.5:c.2439+35C>G MANE Select NP_004351.1:n.2439+35C>G
NM_001317184.2:c.2256+35C>G NP_001304113.1:n.2256+35C>G
NM_001317185.2:c.891+35C>G NP_001304114.1:n.891+35C>G
NM_001317186.2:c.474+35C>G NP_001304115.1:n.474+35C>G