Canonical Allele Identifier: CA396472752
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2445382
ClinVar RCV Id: RCV003154792

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833465T>C , CM000678.2:g.68833465T>C GRCh38
NC_000016.9:g.68867368T>C , CM000678.1:g.68867368T>C GRCh37
NC_000016.8:g.67424869T>C NCBI36
NG_008021.1:g.101174T>C , LRG_301:g.101174T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2615T>C MANE Select ENSP00000261769.4:p.Leu872Pro
ENST00000261769.9:c.2615T>C ENSP00000261769.4:p.Leu872Pro
ENST00000422392.6:c.2432T>C ENSP00000414946.2:p.Leu811Pro
ENST00000562118.1:n.833T>C
ENST00000562836.5:n.2686T>C
ENST00000566510.5:c.*1281T>C ENSP00000458139.1:n.*1281T>C
ENST00000566612.5:c.*855T>C ENSP00000454782.1:n.*855T>C
ENST00000611625.4:c.2678T>C ENSP00000481063.1:p.Leu893Pro
ENST00000612417.4:c.1854-726T>C ENSP00000478360.1:n.1854-726T>C
ENST00000621016.4:c.1866-738T>C ENSP00000480664.1:n.1866-738T>C
NM_004360.3:c.2615T>C , LRG_301t1:c.2615T>C NP_004351.1:p.Leu872Pro
XM_011523488.1:c.1880T>C XP_011521790.1:p.Leu627Pro
XM_011523489.1:c.1880T>C XP_011521791.1:p.Leu627Pro
NM_001317184.1:c.2432T>C NP_001304113.1:p.Leu811Pro
NM_001317185.1:c.1067T>C NP_001304114.1:p.Leu356Pro
NM_001317186.1:c.650T>C NP_001304115.1:p.Leu217Pro
NM_004360.4:c.2615T>C NP_004351.1:p.Leu872Pro
NM_004360.5:c.2615T>C MANE Select NP_004351.1:p.Leu872Pro
NM_001317184.2:c.2432T>C NP_001304113.1:p.Leu811Pro
NM_001317185.2:c.1067T>C NP_001304114.1:p.Leu356Pro
NM_001317186.2:c.650T>C NP_001304115.1:p.Leu217Pro