Canonical Allele Identifier: CA2229974947

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829724C= , CM000678.2:g.68829724C=	GRCh38
NC_000016.9:g.68863627C= , CM000678.1:g.68863627C=	GRCh37
NC_000016.8:g.67421128C=	NCBI36
NG_008021.1:g.97433C= , LRG_301:g.97433C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2366C= MANE Select	ENSP00000261769.4:p.Pro789=
ENST00000261769.9:c.2366C=	ENSP00000261769.4:p.Pro789=
ENST00000422392.6:c.2183C=	ENSP00000414946.2:p.Pro728=
ENST00000562118.1:n.584C=
ENST00000562836.5:n.2437C=
ENST00000566510.5:c.*1032C=	ENSP00000458139.1:n.*1032C=
ENST00000566612.5:c.*606C=	ENSP00000454782.1:n.*606C=
ENST00000611625.4:c.2429C=	ENSP00000481063.1:p.Pro810=
ENST00000612417.4:c.1853+3170C=	ENSP00000478360.1:n.1853+3170C=
ENST00000621016.4:c.1866-4479C=	ENSP00000480664.1:n.1866-4479C=
NM_004360.3:c.2366C= , LRG_301t1:c.2366C=	NP_004351.1:p.Pro789=
XM_011523488.1:c.1631C=	XP_011521790.1:p.Pro544=
XM_011523489.1:c.1631C=	XP_011521791.1:p.Pro544=
NM_001317184.1:c.2183C=	NP_001304113.1:p.Pro728=
NM_001317185.1:c.818C=	NP_001304114.1:p.Pro273=
NM_001317186.1:c.401C=	NP_001304115.1:p.Pro134=
NM_004360.4:c.2366C=	NP_004351.1:p.Pro789=
NM_004360.5:c.2366C= MANE Select	NP_004351.1:p.Pro789=
NM_001317184.2:c.2183C=	NP_001304113.1:p.Pro728=
NM_001317185.2:c.818C=	NP_001304114.1:p.Pro273=
NM_001317186.2:c.401C=	NP_001304115.1:p.Pro134=