Canonical Allele Identifier: CA396458418
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152131015

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810215T>G , CM000678.2:g.68810215T>G GRCh38
NC_000016.9:g.68844118T>G , CM000678.1:g.68844118T>G GRCh37
NC_000016.8:g.67401619T>G NCBI36
NG_008021.1:g.77924T>G , LRG_301:g.77924T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.706T>G MANE Select ENSP00000261769.4:p.Ser236Ala
ENST00000261769.9:c.706T>G ENSP00000261769.4:p.Ser236Ala
ENST00000422392.6:c.706T>G ENSP00000414946.2:p.Ser236Ala
ENST00000561751.1:c.454+1367T>G
ENST00000562836.5:n.777T>G
ENST00000566510.5:c.550T>G ENSP00000458139.1:p.Ser184Ala
ENST00000566612.5:c.706T>G ENSP00000454782.1:p.Ser236Ala
ENST00000611625.4:c.706T>G ENSP00000481063.1:p.Ser236Ala
ENST00000612417.4:c.706T>G ENSP00000478360.1:p.Ser236Ala
ENST00000621016.4:c.706T>G ENSP00000480664.1:p.Ser236Ala
NM_004360.3:c.706T>G , LRG_301t1:c.706T>G NP_004351.1:p.Ser236Ala
XM_011523488.1:c.-30T>G XP_011521790.1:n.-30T>G
XM_011523489.1:c.-30T>G XP_011521791.1:n.-30T>G
NM_001317184.1:c.706T>G NP_001304113.1:p.Ser236Ala
NM_001317185.1:c.-910T>G NP_001304114.1:n.-910T>G
NM_001317186.1:c.-1114T>G NP_001304115.1:n.-1114T>G
NM_004360.4:c.706T>G NP_004351.1:p.Ser236Ala
NM_004360.5:c.706T>G MANE Select NP_004351.1:p.Ser236Ala
NM_001317184.2:c.706T>G NP_001304113.1:p.Ser236Ala
NM_001317185.2:c.-910T>G NP_001304114.1:n.-910T>G
NM_001317186.2:c.-1114T>G NP_001304115.1:n.-1114T>G