Canonical Allele Identifier: CA2229980703

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822140A= , CM000678.2:g.68822140A=	GRCh38
NC_000016.9:g.68856043A= , CM000678.1:g.68856043A=	GRCh37
NC_000016.8:g.67413544A=	NCBI36
NG_008021.1:g.89849A= , LRG_301:g.89849A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1851A= MANE Select	ENSP00000261769.4:p.Ala617=
ENST00000261769.9:c.1851A=	ENSP00000261769.4:p.Ala617=
ENST00000422392.6:c.1668A=	ENSP00000414946.2:p.Ala556=
ENST00000562836.5:n.1922A=
ENST00000566510.5:c.*517A=	ENSP00000458139.1:n.*517A=
ENST00000566612.5:c.*91A=	ENSP00000454782.1:n.*91A=
ENST00000611625.4:c.1914A=	ENSP00000481063.1:p.Ala638=
ENST00000612417.4:c.1830+21A=	ENSP00000478360.1:n.1830+21A=
ENST00000621016.4:c.1851A=	ENSP00000480664.1:p.Ala617=
NM_004360.3:c.1851A= , LRG_301t1:c.1851A=	NP_004351.1:p.Ala617=
XM_011523488.1:c.1116A=	XP_011521790.1:p.Ala372=
XM_011523489.1:c.1116A=	XP_011521791.1:p.Ala372=
NM_001317184.1:c.1668A=	NP_001304113.1:p.Ala556=
NM_001317185.1:c.303A=	NP_001304114.1:p.Ala101=
NM_001317186.1:c.-115A=	NP_001304115.1:n.-115A=
NM_004360.4:c.1851A=	NP_004351.1:p.Ala617=
NM_004360.5:c.1851A= MANE Select	NP_004351.1:p.Ala617=
NM_001317184.2:c.1668A=	NP_001304113.1:p.Ala556=
NM_001317185.2:c.303A=	NP_001304114.1:p.Ala101=
NM_001317186.2:c.-115A=	NP_001304115.1:n.-115A=