Canonical Allele Identifier: CA2229992200

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829694G= , CM000678.2:g.68829694G=	GRCh38
NC_000016.9:g.68863597G= , CM000678.1:g.68863597G=	GRCh37
NC_000016.8:g.67421098G=	NCBI36
NG_008021.1:g.97403G= , LRG_301:g.97403G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2336G= MANE Select	ENSP00000261769.4:p.Arg779=
ENST00000261769.9:c.2336G=	ENSP00000261769.4:p.Arg779=
ENST00000422392.6:c.2153G=	ENSP00000414946.2:p.Arg718=
ENST00000562118.1:n.554G=
ENST00000562836.5:n.2407G=
ENST00000566510.5:c.*1002G=	ENSP00000458139.1:n.*1002G=
ENST00000566612.5:c.*576G=	ENSP00000454782.1:n.*576G=
ENST00000611625.4:c.2399G=	ENSP00000481063.1:p.Arg800=
ENST00000612417.4:c.1853+3140G=	ENSP00000478360.1:n.1853+3140G=
ENST00000621016.4:c.1866-4509G=	ENSP00000480664.1:n.1866-4509G=
NM_004360.3:c.2336G= , LRG_301t1:c.2336G=	NP_004351.1:p.Arg779=
XM_011523488.1:c.1601G=	XP_011521790.1:p.Arg534=
XM_011523489.1:c.1601G=	XP_011521791.1:p.Arg534=
NM_001317184.1:c.2153G=	NP_001304113.1:p.Arg718=
NM_001317185.1:c.788G=	NP_001304114.1:p.Arg263=
NM_001317186.1:c.371G=	NP_001304115.1:p.Arg124=
NM_004360.4:c.2336G=	NP_004351.1:p.Arg779=
NM_004360.5:c.2336G= MANE Select	NP_004351.1:p.Arg779=
NM_001317184.2:c.2153G=	NP_001304113.1:p.Arg718=
NM_001317185.2:c.788G=	NP_001304114.1:p.Arg263=
NM_001317186.2:c.371G=	NP_001304115.1:p.Arg124=