Canonical Allele Identifier: CA496154414
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68853303A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819400A>C , CM000678.2:g.68819400A>C GRCh38
NC_000016.9:g.68853303A>C , CM000678.1:g.68853303A>C GRCh37
NC_000016.8:g.67410804A>C NCBI36
NG_008021.1:g.87109A>C , LRG_301:g.87109A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1686A>C MANE Select ENSP00000261769.4:p.Thr562=
ENST00000261769.9:c.1686A>C ENSP00000261769.4:p.Thr562=
ENST00000422392.6:c.1503A>C ENSP00000414946.2:p.Thr501=
ENST00000562836.5:n.1757A>C
ENST00000566510.5:c.*352A>C ENSP00000458139.1:n.*352A>C
ENST00000566612.5:c.1566-2601A>C ENSP00000454782.1:n.1566-2601A>C
ENST00000611625.4:c.1749A>C ENSP00000481063.1:p.Thr583=
ENST00000612417.4:c.1686A>C ENSP00000478360.1:p.Thr562=
ENST00000621016.4:c.1686A>C ENSP00000480664.1:p.Thr562=
NM_004360.3:c.1686A>C , LRG_301t1:c.1686A>C NP_004351.1:p.Thr562=
XM_011523488.1:c.951A>C XP_011521790.1:p.Thr317=
XM_011523489.1:c.951A>C XP_011521791.1:p.Thr317=
NM_001317184.1:c.1503A>C NP_001304113.1:p.Thr501=
NM_001317185.1:c.138A>C NP_001304114.1:p.Thr46=
NM_001317186.1:c.-254-2601A>C NP_001304115.1:n.-254-2601A>C
NM_004360.4:c.1686A>C NP_004351.1:p.Thr562=
NM_004360.5:c.1686A>C MANE Select NP_004351.1:p.Thr562=
NM_001317184.2:c.1503A>C NP_001304113.1:p.Thr501=
NM_001317185.2:c.138A>C NP_001304114.1:p.Thr46=
NM_001317186.2:c.-254-2601A>C NP_001304115.1:n.-254-2601A>C