Canonical Allele Identifier: CA2229949204

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815688C= , CM000678.2:g.68815688C=	GRCh38
NC_000016.9:g.68849591C= , CM000678.1:g.68849591C=	GRCh37
NC_000016.8:g.67407092C=	NCBI36
NG_008021.1:g.83397C= , LRG_301:g.83397C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1494C= MANE Select	ENSP00000261769.4:p.Asp498=
ENST00000261769.9:c.1494C=	ENSP00000261769.4:p.Asp498=
ENST00000422392.6:c.1311C=	ENSP00000414946.2:p.Asp437=
ENST00000562836.5:n.1565C=
ENST00000566510.5:c.*160C=	ENSP00000458139.1:n.*160C=
ENST00000566612.5:c.1494C=	ENSP00000454782.1:p.Asp498=
ENST00000611625.4:c.1557C=	ENSP00000481063.1:p.Asp519=
ENST00000612417.4:c.1494C=	ENSP00000478360.1:p.Asp498=
ENST00000621016.4:c.1494C=	ENSP00000480664.1:p.Asp498=
NM_004360.3:c.1494C= , LRG_301t1:c.1494C=	NP_004351.1:p.Asp498=
XM_011523488.1:c.759C=	XP_011521790.1:p.Asp253=
XM_011523489.1:c.759C=	XP_011521791.1:p.Asp253=
NM_001317184.1:c.1311C=	NP_001304113.1:p.Asp437=
NM_001317185.1:c.-55C=	NP_001304114.1:n.-55C=
NM_001317186.1:c.-326C=	NP_001304115.1:n.-326C=
NM_004360.4:c.1494C=	NP_004351.1:p.Asp498=
NM_004360.5:c.1494C= MANE Select	NP_004351.1:p.Asp498=
NM_001317184.2:c.1311C=	NP_001304113.1:p.Asp437=
NM_001317185.2:c.-55C=	NP_001304114.1:n.-55C=
NM_001317186.2:c.-326C=	NP_001304115.1:n.-326C=