Canonical Allele Identifier: CA396472861
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152144236

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833480G>A , CM000678.2:g.68833480G>A GRCh38
NC_000016.9:g.68867383G>A , CM000678.1:g.68867383G>A GRCh37
NC_000016.8:g.67424884G>A NCBI36
NG_008021.1:g.101189G>A , LRG_301:g.101189G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2630G>A MANE Select ENSP00000261769.4:p.Gly877Glu
ENST00000261769.9:c.2630G>A ENSP00000261769.4:p.Gly877Glu
ENST00000422392.6:c.2447G>A ENSP00000414946.2:p.Gly816Glu
ENST00000562118.1:n.848G>A
ENST00000562836.5:n.2701G>A
ENST00000566510.5:c.*1296G>A ENSP00000458139.1:n.*1296G>A
ENST00000566612.5:c.*870G>A ENSP00000454782.1:n.*870G>A
ENST00000611625.4:c.2693G>A ENSP00000481063.1:p.Gly898Glu
ENST00000612417.4:c.1854-711G>A ENSP00000478360.1:n.1854-711G>A
ENST00000621016.4:c.1866-723G>A ENSP00000480664.1:n.1866-723G>A
NM_004360.3:c.2630G>A , LRG_301t1:c.2630G>A NP_004351.1:p.Gly877Glu
XM_011523488.1:c.1895G>A XP_011521790.1:p.Gly632Glu
XM_011523489.1:c.1895G>A XP_011521791.1:p.Gly632Glu
NM_001317184.1:c.2447G>A NP_001304113.1:p.Gly816Glu
NM_001317185.1:c.1082G>A NP_001304114.1:p.Gly361Glu
NM_001317186.1:c.665G>A NP_001304115.1:p.Gly222Glu
NM_004360.4:c.2630G>A NP_004351.1:p.Gly877Glu
NM_004360.5:c.2630G>A MANE Select NP_004351.1:p.Gly877Glu
NM_001317184.2:c.2447G>A NP_001304113.1:p.Gly816Glu
NM_001317185.2:c.1082G>A NP_001304114.1:p.Gly361Glu
NM_001317186.2:c.665G>A NP_001304115.1:p.Gly222Glu