Canonical Allele Identifier: CA2229983188

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823542G= , CM000678.2:g.68823542G=	GRCh38
NC_000016.9:g.68857445G= , CM000678.1:g.68857445G=	GRCh37
NC_000016.8:g.67414946G=	NCBI36
NG_008021.1:g.91251G= , LRG_301:g.91251G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2080G= MANE Select	ENSP00000261769.4:p.Val694=
ENST00000261769.9:c.2080G=	ENSP00000261769.4:p.Val694=
ENST00000422392.6:c.1897G=	ENSP00000414946.2:p.Val633=
ENST00000562118.1:n.298G=
ENST00000562836.5:n.2151G=
ENST00000566510.5:c.*746G=	ENSP00000458139.1:n.*746G=
ENST00000566612.5:c.*320G=	ENSP00000454782.1:n.*320G=
ENST00000611625.4:c.2143G=	ENSP00000481063.1:p.Val715=
ENST00000612417.4:c.1830+1423G=	ENSP00000478360.1:n.1830+1423G=
ENST00000621016.4:c.1865+1388G=	ENSP00000480664.1:n.1865+1388G=
NM_004360.3:c.2080G= , LRG_301t1:c.2080G=	NP_004351.1:p.Val694=
XM_011523488.1:c.1345G=	XP_011521790.1:p.Val449=
XM_011523489.1:c.1345G=	XP_011521791.1:p.Val449=
NM_001317184.1:c.1897G=	NP_001304113.1:p.Val633=
NM_001317185.1:c.532G=	NP_001304114.1:p.Val178=
NM_001317186.1:c.115G=	NP_001304115.1:p.Val39=
NM_004360.4:c.2080G=	NP_004351.1:p.Val694=
NM_004360.5:c.2080G= MANE Select	NP_004351.1:p.Val694=
NM_001317184.2:c.1897G=	NP_001304113.1:p.Val633=
NM_001317185.2:c.532G=	NP_001304114.1:p.Val178=
NM_001317186.2:c.115G=	NP_001304115.1:p.Val39=