Canonical Allele Identifier: CA2229982678

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823437G= , CM000678.2:g.68823437G=	GRCh38
NC_000016.9:g.68857340G= , CM000678.1:g.68857340G=	GRCh37
NC_000016.8:g.67414841G=	NCBI36
NG_008021.1:g.91146G= , LRG_301:g.91146G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1975G= MANE Select	ENSP00000261769.4:p.Glu659=
ENST00000261769.9:c.1975G=	ENSP00000261769.4:p.Glu659=
ENST00000422392.6:c.1792G=	ENSP00000414946.2:p.Glu598=
ENST00000562118.1:n.193G=
ENST00000562836.5:n.2046G=
ENST00000566510.5:c.*641G=	ENSP00000458139.1:n.*641G=
ENST00000566612.5:c.*215G=	ENSP00000454782.1:n.*215G=
ENST00000611625.4:c.2038G=	ENSP00000481063.1:p.Glu680=
ENST00000612417.4:c.1830+1318G=	ENSP00000478360.1:n.1830+1318G=
ENST00000621016.4:c.1865+1283G=	ENSP00000480664.1:n.1865+1283G=
NM_004360.3:c.1975G= , LRG_301t1:c.1975G=	NP_004351.1:p.Glu659=
XM_011523488.1:c.1240G=	XP_011521790.1:p.Glu414=
XM_011523489.1:c.1240G=	XP_011521791.1:p.Glu414=
NM_001317184.1:c.1792G=	NP_001304113.1:p.Glu598=
NM_001317185.1:c.427G=	NP_001304114.1:p.Glu143=
NM_001317186.1:c.10G=	NP_001304115.1:p.Glu4=
NM_004360.4:c.1975G=	NP_004351.1:p.Glu659=
NM_004360.5:c.1975G= MANE Select	NP_004351.1:p.Glu659=
NM_001317184.2:c.1792G=	NP_001304113.1:p.Glu598=
NM_001317185.2:c.427G=	NP_001304114.1:p.Glu143=
NM_001317186.2:c.10G=	NP_001304115.1:p.Glu4=