Canonical Allele Identifier: CA2576038676
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs535931444

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819218C>G , CM000678.2:g.68819218C>G GRCh38
NC_000016.9:g.68853121C>G , CM000678.1:g.68853121C>G GRCh37
NC_000016.8:g.67410622C>G NCBI36
NG_008021.1:g.86927C>G , LRG_301:g.86927C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1566-62C>G MANE Select ENSP00000261769.4:n.1566-62C>G
ENST00000261769.9:c.1566-62C>G ENSP00000261769.4:n.1566-62C>G
ENST00000422392.6:c.1383-62C>G ENSP00000414946.2:n.1383-62C>G
ENST00000562836.5:n.1637-62C>G
ENST00000566510.5:c.*232-62C>G ENSP00000458139.1:n.*232-62C>G
ENST00000566612.5:c.1566-2783C>G ENSP00000454782.1:n.1566-2783C>G
ENST00000611625.4:c.1629-62C>G ENSP00000481063.1:n.1629-62C>G
ENST00000612417.4:c.1566-62C>G ENSP00000478360.1:n.1566-62C>G
ENST00000621016.4:c.1566-62C>G ENSP00000480664.1:n.1566-62C>G
NM_004360.3:c.1566-62C>G , LRG_301t1:c.1566-62C>G NP_004351.1:n.1566-62C>G
XM_011523488.1:c.831-62C>G XP_011521790.1:n.831-62C>G
XM_011523489.1:c.831-62C>G XP_011521791.1:n.831-62C>G
NM_001317184.1:c.1383-62C>G NP_001304113.1:n.1383-62C>G
NM_001317185.1:c.18-62C>G NP_001304114.1:n.18-62C>G
NM_001317186.1:c.-254-2783C>G NP_001304115.1:n.-254-2783C>G
NM_004360.4:c.1566-62C>G NP_004351.1:n.1566-62C>G
NM_004360.5:c.1566-62C>G MANE Select NP_004351.1:n.1566-62C>G
NM_001317184.2:c.1383-62C>G NP_001304113.1:n.1383-62C>G
NM_001317185.2:c.18-62C>G NP_001304114.1:n.18-62C>G
NM_001317186.2:c.-254-2783C>G NP_001304115.1:n.-254-2783C>G