Canonical Allele Identifier: CA396451341
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2703400
ClinVar RCV Id: RCV003512869
dbSNP Id: rs1555509646

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737441C>G , CM000678.2:g.68737441C>G GRCh38
NC_000016.9:g.68771344C>G , CM000678.1:g.68771344C>G GRCh37
NC_000016.8:g.67328845C>G NCBI36
NG_008021.1:g.5150C>G , LRG_301:g.5150C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.26C>G MANE Select ENSP00000261769.4:p.Ser9Trp
ENST00000261769.9:c.26C>G ENSP00000261769.4:p.Ser9Trp
ENST00000422392.6:c.26C>G ENSP00000414946.2:p.Ser9Trp
ENST00000566510.5:c.26C>G ENSP00000458139.1:p.Ser9Trp
ENST00000566612.5:c.26C>G ENSP00000454782.1:p.Ser9Trp
ENST00000611625.4:c.26C>G ENSP00000481063.1:p.Ser9Trp
ENST00000612417.4:c.26C>G ENSP00000478360.1:p.Ser9Trp
ENST00000621016.4:c.26C>G ENSP00000480664.1:p.Ser9Trp
NM_004360.3:c.26C>G , LRG_301t1:c.26C>G NP_004351.1:p.Ser9Trp
NM_001317184.1:c.26C>G NP_001304113.1:p.Ser9Trp
NM_001317185.1:c.-1590C>G NP_001304114.1:n.-1590C>G
NM_001317186.1:c.-1794C>G NP_001304115.1:n.-1794C>G
NM_004360.4:c.26C>G NP_004351.1:p.Ser9Trp
NM_004360.5:c.26C>G MANE Select NP_004351.1:p.Ser9Trp
NM_001317184.2:c.26C>G NP_001304113.1:p.Ser9Trp
NM_001317185.2:c.-1590C>G NP_001304114.1:n.-1590C>G
NM_001317186.2:c.-1794C>G NP_001304115.1:n.-1794C>G