Canonical Allele Identifier: CA2229978145

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68819402C= , CM000678.2:g.68819402C=	GRCh38
NC_000016.9:g.68853305C= , CM000678.1:g.68853305C=	GRCh37
NC_000016.8:g.67410806C=	NCBI36
NG_008021.1:g.87111C= , LRG_301:g.87111C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1688C= MANE Select	ENSP00000261769.4:p.Ala563=
ENST00000261769.9:c.1688C=	ENSP00000261769.4:p.Ala563=
ENST00000422392.6:c.1505C=	ENSP00000414946.2:p.Ala502=
ENST00000562836.5:n.1759C=
ENST00000566510.5:c.*354C=	ENSP00000458139.1:n.*354C=
ENST00000566612.5:c.1566-2599C=	ENSP00000454782.1:n.1566-2599C=
ENST00000611625.4:c.1751C=	ENSP00000481063.1:p.Ala584=
ENST00000612417.4:c.1688C=	ENSP00000478360.1:p.Ala563=
ENST00000621016.4:c.1688C=	ENSP00000480664.1:p.Ala563=
NM_004360.3:c.1688C= , LRG_301t1:c.1688C=	NP_004351.1:p.Ala563=
XM_011523488.1:c.953C=	XP_011521790.1:p.Ala318=
XM_011523489.1:c.953C=	XP_011521791.1:p.Ala318=
NM_001317184.1:c.1505C=	NP_001304113.1:p.Ala502=
NM_001317185.1:c.140C=	NP_001304114.1:p.Ala47=
NM_001317186.1:c.-254-2599C=	NP_001304115.1:n.-254-2599C=
NM_004360.4:c.1688C=	NP_004351.1:p.Ala563=
NM_004360.5:c.1688C= MANE Select	NP_004351.1:p.Ala563=
NM_001317184.2:c.1505C=	NP_001304113.1:p.Ala502=
NM_001317185.2:c.140C=	NP_001304114.1:p.Ala47=
NM_001317186.2:c.-254-2599C=	NP_001304115.1:n.-254-2599C=