Canonical Allele Identifier: CA496154311
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68853204T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819301T>A , CM000678.2:g.68819301T>A GRCh38
NC_000016.9:g.68853204T>A , CM000678.1:g.68853204T>A GRCh37
NC_000016.8:g.67410705T>A NCBI36
NG_008021.1:g.87010T>A , LRG_301:g.87010T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1587T>A MANE Select ENSP00000261769.4:p.Thr529=
ENST00000261769.9:c.1587T>A ENSP00000261769.4:p.Thr529=
ENST00000422392.6:c.1404T>A ENSP00000414946.2:p.Thr468=
ENST00000562836.5:n.1658T>A
ENST00000566510.5:c.*253T>A ENSP00000458139.1:p.=
ENST00000566612.5:c.1566-2700T>A ENSP00000454782.1:p.=
ENST00000611625.4:c.1650T>A ENSP00000481063.1:p.Thr550=
ENST00000612417.4:c.1587T>A ENSP00000478360.1:p.Thr529=
ENST00000621016.4:c.1587T>A ENSP00000480664.1:p.Thr529=
NM_004360.3:c.1587T>A , LRG_301t1:c.1587T>A NP_004351.1:p.Thr529=
XM_011523488.1:c.852T>A XP_011521790.1:p.Thr284=
XM_011523489.1:c.852T>A XP_011521791.1:p.Thr284=
NM_001317184.1:c.1404T>A NP_001304113.1:p.Thr468=
NM_001317185.1:c.39T>A NP_001304114.1:p.Thr13=
NM_001317186.1:c.-254-2700T>A NP_001304115.1:p.=
NM_004360.4:c.1587T>A NP_004351.1:p.Thr529=
NM_004360.5:c.1587T>A MANE Select NP_004351.1:p.Thr529=
NM_001317184.2:c.1404T>A NP_001304113.1:p.Thr468=
NM_001317185.2:c.39T>A NP_001304114.1:p.Thr13=
NM_001317186.2:c.-254-2700T>A NP_001304115.1:p.=