Canonical Allele Identifier: CA496152760
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1670841
ClinVar RCV Id: RCV002196212
dbSNP Id: rs1555515428
MyVariant Identifiers: chr16:g.68844114T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810211T>C , CM000678.2:g.68810211T>C GRCh38
NC_000016.9:g.68844114T>C , CM000678.1:g.68844114T>C GRCh37
NC_000016.8:g.67401615T>C NCBI36
NG_008021.1:g.77920T>C , LRG_301:g.77920T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.702T>C MANE Select ENSP00000261769.4:p.Ala234=
ENST00000261769.9:c.702T>C ENSP00000261769.4:p.Ala234=
ENST00000422392.6:c.702T>C ENSP00000414946.2:p.Ala234=
ENST00000561751.1:c.454+1363T>C
ENST00000562836.5:n.773T>C
ENST00000566510.5:c.546T>C ENSP00000458139.1:p.Ala182=
ENST00000566612.5:c.702T>C ENSP00000454782.1:p.Ala234=
ENST00000611625.4:c.702T>C ENSP00000481063.1:p.Ala234=
ENST00000612417.4:c.702T>C ENSP00000478360.1:p.Ala234=
ENST00000621016.4:c.702T>C ENSP00000480664.1:p.Ala234=
NM_004360.3:c.702T>C , LRG_301t1:c.702T>C NP_004351.1:p.Ala234=
XM_011523488.1:c.-34T>C XP_011521790.1:n.-34T>C
XM_011523489.1:c.-34T>C XP_011521791.1:n.-34T>C
NM_001317184.1:c.702T>C NP_001304113.1:p.Ala234=
NM_001317185.1:c.-914T>C NP_001304114.1:n.-914T>C
NM_001317186.1:c.-1118T>C NP_001304115.1:n.-1118T>C
NM_004360.4:c.702T>C NP_004351.1:p.Ala234=
NM_004360.5:c.702T>C MANE Select NP_004351.1:p.Ala234=
NM_001317184.2:c.702T>C NP_001304113.1:p.Ala234=
NM_001317185.2:c.-914T>C NP_001304114.1:n.-914T>C
NM_001317186.2:c.-1118T>C NP_001304115.1:n.-1118T>C