Canonical Allele Identifier: CA496392514

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68855926_68855927insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822023_68822024insC , CM000678.2:g.68822023_68822024insC	GRCh38
NC_000016.9:g.68855926_68855927insC , CM000678.1:g.68855926_68855927insC	GRCh37
NC_000016.8:g.67413427_67413428insC	NCBI36
NG_008021.1:g.89732_89733insC , LRG_301:g.89732_89733insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1734_1735insC MANE Select	ENSP00000261769.4:p.Gly579ArgfsTer9
ENST00000261769.9:c.1734_1735insC	ENSP00000261769.4:p.Gly579ArgfsTer9
ENST00000422392.6:c.1551_1552insC	ENSP00000414946.2:p.Gly518ArgfsTer9
ENST00000562836.5:n.1805_1806insC
ENST00000566510.5:c.*400_*401insC	ENSP00000458139.1:n.*400_*401insC
ENST00000566612.5:c.1588_1589insC	ENSP00000454782.1:p.Arg530ThrfsTer6
ENST00000611625.4:c.1797_1798insC	ENSP00000481063.1:p.Gly600ArgfsTer9
ENST00000612417.4:c.1734_1735insC	ENSP00000478360.1:p.Gly579ArgfsTer9
ENST00000621016.4:c.1734_1735insC	ENSP00000480664.1:p.Gly579ArgfsTer9
NM_004360.3:c.1734_1735insC , LRG_301t1:c.1734_1735insC	NP_004351.1:p.Gly579ArgfsTer9
XM_011523488.1:c.999_1000insC	XP_011521790.1:p.Gly334ArgfsTer9
XM_011523489.1:c.999_1000insC	XP_011521791.1:p.Gly334ArgfsTer9
NM_001317184.1:c.1551_1552insC	NP_001304113.1:p.Gly518ArgfsTer9
NM_001317185.1:c.186_187insC	NP_001304114.1:p.Gly63ArgfsTer9
NM_001317186.1:c.-232_-231insC	NP_001304115.1:n.-232_-231insC
NM_004360.4:c.1734_1735insC	NP_004351.1:p.Gly579ArgfsTer9
NM_004360.5:c.1734_1735insC MANE Select	NP_004351.1:p.Gly579ArgfsTer9
NM_001317184.2:c.1551_1552insC	NP_001304113.1:p.Gly518ArgfsTer9
NM_001317185.2:c.186_187insC	NP_001304114.1:p.Gly63ArgfsTer9
NM_001317186.2:c.-232_-231insC	NP_001304115.1:n.-232_-231insC