Canonical Allele Identifier: CA2229992059

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829674G= , CM000678.2:g.68829674G=	GRCh38
NC_000016.9:g.68863577G= , CM000678.1:g.68863577G=	GRCh37
NC_000016.8:g.67421078G=	NCBI36
NG_008021.1:g.97383G= , LRG_301:g.97383G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2316G= MANE Select	ENSP00000261769.4:p.Leu772=
ENST00000261769.9:c.2316G=	ENSP00000261769.4:p.Leu772=
ENST00000422392.6:c.2133G=	ENSP00000414946.2:p.Leu711=
ENST00000562118.1:n.534G=
ENST00000562836.5:n.2387G=
ENST00000566510.5:c.*982G=	ENSP00000458139.1:n.*982G=
ENST00000566612.5:c.*556G=	ENSP00000454782.1:n.*556G=
ENST00000611625.4:c.2379G=	ENSP00000481063.1:p.Leu793=
ENST00000612417.4:c.1853+3120G=	ENSP00000478360.1:n.1853+3120G=
ENST00000621016.4:c.1866-4529G=	ENSP00000480664.1:n.1866-4529G=
NM_004360.3:c.2316G= , LRG_301t1:c.2316G=	NP_004351.1:p.Leu772=
XM_011523488.1:c.1581G=	XP_011521790.1:p.Leu527=
XM_011523489.1:c.1581G=	XP_011521791.1:p.Leu527=
NM_001317184.1:c.2133G=	NP_001304113.1:p.Leu711=
NM_001317185.1:c.768G=	NP_001304114.1:p.Leu256=
NM_001317186.1:c.351G=	NP_001304115.1:p.Leu117=
NM_004360.4:c.2316G=	NP_004351.1:p.Leu772=
NM_004360.5:c.2316G= MANE Select	NP_004351.1:p.Leu772=
NM_001317184.2:c.2133G=	NP_001304113.1:p.Leu711=
NM_001317185.2:c.768G=	NP_001304114.1:p.Leu256=
NM_001317186.2:c.351G=	NP_001304115.1:p.Leu117=