Canonical Allele Identifier: CA2229978380

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833423A= , CM000678.2:g.68833423A=	GRCh38
NC_000016.9:g.68867326A= , CM000678.1:g.68867326A=	GRCh37
NC_000016.8:g.67424827A=	NCBI36
NG_008021.1:g.101132A= , LRG_301:g.101132A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2573A= MANE Select	ENSP00000261769.4:p.Asp858=
ENST00000261769.9:c.2573A=	ENSP00000261769.4:p.Asp858=
ENST00000422392.6:c.2390A=	ENSP00000414946.2:p.Asp797=
ENST00000562118.1:n.791A=
ENST00000562836.5:n.2644A=
ENST00000566510.5:c.*1239A=	ENSP00000458139.1:n.*1239A=
ENST00000566612.5:c.*813A=	ENSP00000454782.1:n.*813A=
ENST00000611625.4:c.2636A=	ENSP00000481063.1:p.Asp879=
ENST00000612417.4:c.1854-768A=	ENSP00000478360.1:n.1854-768A=
ENST00000621016.4:c.1866-780A=	ENSP00000480664.1:n.1866-780A=
NM_004360.3:c.2573A= , LRG_301t1:c.2573A=	NP_004351.1:p.Asp858=
XM_011523488.1:c.1838A=	XP_011521790.1:p.Asp613=
XM_011523489.1:c.1838A=	XP_011521791.1:p.Asp613=
NM_001317184.1:c.2390A=	NP_001304113.1:p.Asp797=
NM_001317185.1:c.1025A=	NP_001304114.1:p.Asp342=
NM_001317186.1:c.608A=	NP_001304115.1:p.Asp203=
NM_004360.4:c.2573A=	NP_004351.1:p.Asp858=
NM_004360.5:c.2573A= MANE Select	NP_004351.1:p.Asp858=
NM_001317184.2:c.2390A=	NP_001304113.1:p.Asp797=
NM_001317185.2:c.1025A=	NP_001304114.1:p.Asp342=
NM_001317186.2:c.608A=	NP_001304115.1:p.Asp203=