Canonical Allele Identifier: CA496152759
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1756790
ClinVar RCV Id: RCV002364931
dbSNP Id: rs1555515428
MyVariant Identifiers: chr16:g.68844114T>A (hg19)

Genomic Alleles

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

Transcript Alleles

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