Canonical Allele Identifier: CA2229969058

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68811824G= , CM000678.2:g.68811824G=	GRCh38
NC_000016.9:g.68845727G= , CM000678.1:g.68845727G=	GRCh37
NC_000016.8:g.67403228G=	NCBI36
NG_008021.1:g.79533G= , LRG_301:g.79533G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.973G= MANE Select	ENSP00000261769.4:p.Val325=
ENST00000261769.9:c.973G=	ENSP00000261769.4:p.Val325=
ENST00000422392.6:c.973G=	ENSP00000414946.2:p.Val325=
ENST00000561751.1:c.595G=
ENST00000562836.5:n.1044G=
ENST00000566510.5:c.817G=	ENSP00000458139.1:p.Val273=
ENST00000566612.5:c.973G=	ENSP00000454782.1:p.Val325=
ENST00000611625.4:c.973G=	ENSP00000481063.1:p.Val325=
ENST00000612417.4:c.973G=	ENSP00000478360.1:p.Val325=
ENST00000621016.4:c.973G=	ENSP00000480664.1:p.Val325=
NM_004360.3:c.973G= , LRG_301t1:c.973G=	NP_004351.1:p.Val325=
XM_011523488.1:c.238G=	XP_011521790.1:p.Val80=
XM_011523489.1:c.238G=	XP_011521791.1:p.Val80=
NM_001317184.1:c.973G=	NP_001304113.1:p.Val325=
NM_001317185.1:c.-643G=	NP_001304114.1:n.-643G=
NM_001317186.1:c.-847G=	NP_001304115.1:n.-847G=
NM_004360.4:c.973G=	NP_004351.1:p.Val325=
NM_004360.5:c.973G= MANE Select	NP_004351.1:p.Val325=
NM_001317184.2:c.973G=	NP_001304113.1:p.Val325=
NM_001317185.2:c.-643G=	NP_001304114.1:n.-643G=
NM_001317186.2:c.-847G=	NP_001304115.1:n.-847G=