Canonical Allele Identifier: CA2229975186

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829774G= , CM000678.2:g.68829774G=	GRCh38
NC_000016.9:g.68863677G= , CM000678.1:g.68863677G=	GRCh37
NC_000016.8:g.67421178G=	NCBI36
NG_008021.1:g.97483G= , LRG_301:g.97483G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2416G= MANE Select	ENSP00000261769.4:p.Glu806=
ENST00000261769.9:c.2416G=	ENSP00000261769.4:p.Glu806=
ENST00000422392.6:c.2233G=	ENSP00000414946.2:p.Glu745=
ENST00000562118.1:n.634G=
ENST00000562836.5:n.2487G=
ENST00000566510.5:c.*1082G=	ENSP00000458139.1:n.*1082G=
ENST00000566612.5:c.*656G=	ENSP00000454782.1:n.*656G=
ENST00000611625.4:c.2479G=	ENSP00000481063.1:p.Glu827=
ENST00000612417.4:c.1853+3220G=	ENSP00000478360.1:n.1853+3220G=
ENST00000621016.4:c.1866-4429G=	ENSP00000480664.1:n.1866-4429G=
NM_004360.3:c.2416G= , LRG_301t1:c.2416G=	NP_004351.1:p.Glu806=
XM_011523488.1:c.1681G=	XP_011521790.1:p.Glu561=
XM_011523489.1:c.1681G=	XP_011521791.1:p.Glu561=
NM_001317184.1:c.2233G=	NP_001304113.1:p.Glu745=
NM_001317185.1:c.868G=	NP_001304114.1:p.Glu290=
NM_001317186.1:c.451G=	NP_001304115.1:p.Glu151=
NM_004360.4:c.2416G=	NP_004351.1:p.Glu806=
NM_004360.5:c.2416G= MANE Select	NP_004351.1:p.Glu806=
NM_001317184.2:c.2233G=	NP_001304113.1:p.Glu745=
NM_001317185.2:c.868G=	NP_001304114.1:p.Glu290=
NM_001317186.2:c.451G=	NP_001304115.1:p.Glu151=