Canonical Allele Identifier: CA2229980552

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822087A= , CM000678.2:g.68822087A=	GRCh38
NC_000016.9:g.68855990A= , CM000678.1:g.68855990A=	GRCh37
NC_000016.8:g.67413491A=	NCBI36
NG_008021.1:g.89796A= , LRG_301:g.89796A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1798A= MANE Select	ENSP00000261769.4:p.Ile600=
ENST00000261769.9:c.1798A=	ENSP00000261769.4:p.Ile600=
ENST00000422392.6:c.1615A=	ENSP00000414946.2:p.Ile539=
ENST00000562836.5:n.1869A=
ENST00000566510.5:c.*464A=	ENSP00000458139.1:n.*464A=
ENST00000566612.5:c.*38A=	ENSP00000454782.1:n.*38A=
ENST00000611625.4:c.1861A=	ENSP00000481063.1:p.Ile621=
ENST00000612417.4:c.1798A=	ENSP00000478360.1:p.Ile600=
ENST00000621016.4:c.1798A=	ENSP00000480664.1:p.Ile600=
NM_004360.3:c.1798A= , LRG_301t1:c.1798A=	NP_004351.1:p.Ile600=
XM_011523488.1:c.1063A=	XP_011521790.1:p.Ile355=
XM_011523489.1:c.1063A=	XP_011521791.1:p.Ile355=
NM_001317184.1:c.1615A=	NP_001304113.1:p.Ile539=
NM_001317185.1:c.250A=	NP_001304114.1:p.Ile84=
NM_001317186.1:c.-168A=	NP_001304115.1:n.-168A=
NM_004360.4:c.1798A=	NP_004351.1:p.Ile600=
NM_004360.5:c.1798A= MANE Select	NP_004351.1:p.Ile600=
NM_001317184.2:c.1615A=	NP_001304113.1:p.Ile539=
NM_001317185.2:c.250A=	NP_001304114.1:p.Ile84=
NM_001317186.2:c.-168A=	NP_001304115.1:n.-168A=