Canonical Allele Identifier: CA496157414

Gene: CDH1

Linked Data

• dbSNP Id: rs1555517848
• gnomAD v4: 16-68829707-T-C
• MyVariant Identifiers: chr16:g.68863610T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829707T>C , CM000678.2:g.68829707T>C	GRCh38
NC_000016.9:g.68863610T>C , CM000678.1:g.68863610T>C	GRCh37
NC_000016.8:g.67421111T>C	NCBI36
NG_008021.1:g.97416T>C , LRG_301:g.97416T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2349T>C MANE Select	ENSP00000261769.4:p.Thr783=
ENST00000261769.9:c.2349T>C	ENSP00000261769.4:p.Thr783=
ENST00000422392.6:c.2166T>C	ENSP00000414946.2:p.Thr722=
ENST00000562118.1:n.567T>C
ENST00000562836.5:n.2420T>C
ENST00000566510.5:c.*1015T>C	ENSP00000458139.1:n.*1015T>C
ENST00000566612.5:c.*589T>C	ENSP00000454782.1:n.*589T>C
ENST00000611625.4:c.2412T>C	ENSP00000481063.1:p.Thr804=
ENST00000612417.4:c.1853+3153T>C	ENSP00000478360.1:n.1853+3153T>C
ENST00000621016.4:c.1866-4496T>C	ENSP00000480664.1:n.1866-4496T>C
NM_004360.3:c.2349T>C , LRG_301t1:c.2349T>C	NP_004351.1:p.Thr783=
XM_011523488.1:c.1614T>C	XP_011521790.1:p.Thr538=
XM_011523489.1:c.1614T>C	XP_011521791.1:p.Thr538=
NM_001317184.1:c.2166T>C	NP_001304113.1:p.Thr722=
NM_001317185.1:c.801T>C	NP_001304114.1:p.Thr267=
NM_001317186.1:c.384T>C	NP_001304115.1:p.Thr128=
NM_004360.4:c.2349T>C	NP_004351.1:p.Thr783=
NM_004360.5:c.2349T>C MANE Select	NP_004351.1:p.Thr783=
NM_001317184.2:c.2166T>C	NP_001304113.1:p.Thr722=
NM_001317185.2:c.801T>C	NP_001304114.1:p.Thr267=
NM_001317186.2:c.384T>C	NP_001304115.1:p.Thr128=