Canonical Allele Identifier: CA396467065

Gene: CDH1

Linked Data

• dbSNP Id: rs1596963727
• MyVariant Identifiers: chr16:g.68856059A>C (hg19) ; chr16:g.68822156A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822156A>C , CM000678.2:g.68822156A>C	GRCh38
NC_000016.9:g.68856059A>C , CM000678.1:g.68856059A>C	GRCh37
NC_000016.8:g.67413560A>C	NCBI36
NG_008021.1:g.89865A>C , LRG_301:g.89865A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1867A>C MANE Select	ENSP00000261769.4:p.Thr623Pro
ENST00000261769.9:c.1867A>C	ENSP00000261769.4:p.Thr623Pro
ENST00000422392.6:c.1684A>C	ENSP00000414946.2:p.Thr562Pro
ENST00000562836.5:n.1938A>C
ENST00000566510.5:c.*533A>C	ENSP00000458139.1:n.*533A>C
ENST00000566612.5:c.*107A>C	ENSP00000454782.1:n.*107A>C
ENST00000611625.4:c.1930A>C	ENSP00000481063.1:p.Thr644Pro
ENST00000612417.4:c.1830+37A>C	ENSP00000478360.1:n.1830+37A>C
ENST00000621016.4:c.1865+2A>C	ENSP00000480664.1:n.1865+2A>C
NM_004360.3:c.1867A>C , LRG_301t1:c.1867A>C	NP_004351.1:p.Thr623Pro
XM_011523488.1:c.1132A>C	XP_011521790.1:p.Thr378Pro
XM_011523489.1:c.1132A>C	XP_011521791.1:p.Thr378Pro
NM_001317184.1:c.1684A>C	NP_001304113.1:p.Thr562Pro
NM_001317185.1:c.319A>C	NP_001304114.1:p.Thr107Pro
NM_001317186.1:c.-99A>C	NP_001304115.1:n.-99A>C
NM_004360.4:c.1867A>C	NP_004351.1:p.Thr623Pro
NM_004360.5:c.1867A>C MANE Select	NP_004351.1:p.Thr623Pro
NM_001317184.2:c.1684A>C	NP_001304113.1:p.Thr562Pro
NM_001317185.2:c.319A>C	NP_001304114.1:p.Thr107Pro
NM_001317186.2:c.-99A>C	NP_001304115.1:n.-99A>C