Canonical Allele Identifier: CA2229975277

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829796A= , CM000678.2:g.68829796A=	GRCh38
NC_000016.9:g.68863699A= , CM000678.1:g.68863699A=	GRCh37
NC_000016.8:g.67421200A=	NCBI36
NG_008021.1:g.97505A= , LRG_301:g.97505A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2438A= MANE Select	ENSP00000261769.4:p.Glu813=
ENST00000261769.9:c.2438A=	ENSP00000261769.4:p.Glu813=
ENST00000422392.6:c.2255A=	ENSP00000414946.2:p.Glu752=
ENST00000562118.1:n.656A=
ENST00000562836.5:n.2509A=
ENST00000566510.5:c.*1104A=	ENSP00000458139.1:n.*1104A=
ENST00000566612.5:c.*678A=	ENSP00000454782.1:n.*678A=
ENST00000611625.4:c.2501A=	ENSP00000481063.1:p.Glu834=
ENST00000612417.4:c.1853+3242A=	ENSP00000478360.1:n.1853+3242A=
ENST00000621016.4:c.1866-4407A=	ENSP00000480664.1:n.1866-4407A=
NM_004360.3:c.2438A= , LRG_301t1:c.2438A=	NP_004351.1:p.Glu813=
XM_011523488.1:c.1703A=	XP_011521790.1:p.Glu568=
XM_011523489.1:c.1703A=	XP_011521791.1:p.Glu568=
NM_001317184.1:c.2255A=	NP_001304113.1:p.Glu752=
NM_001317185.1:c.890A=	NP_001304114.1:p.Glu297=
NM_001317186.1:c.473A=	NP_001304115.1:p.Glu158=
NM_004360.4:c.2438A=	NP_004351.1:p.Glu813=
NM_004360.5:c.2438A= MANE Select	NP_004351.1:p.Glu813=
NM_001317184.2:c.2255A=	NP_001304113.1:p.Glu752=
NM_001317185.2:c.890A=	NP_001304114.1:p.Glu297=
NM_001317186.2:c.473A=	NP_001304115.1:p.Glu158=