Canonical Allele Identifier: CA2229983185

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823541C= , CM000678.2:g.68823541C=	GRCh38
NC_000016.9:g.68857444C= , CM000678.1:g.68857444C=	GRCh37
NC_000016.8:g.67414945C=	NCBI36
NG_008021.1:g.91250C= , LRG_301:g.91250C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2079C= MANE Select	ENSP00000261769.4:p.Gly693=
ENST00000261769.9:c.2079C=	ENSP00000261769.4:p.Gly693=
ENST00000422392.6:c.1896C=	ENSP00000414946.2:p.Gly632=
ENST00000562118.1:n.297C=
ENST00000562836.5:n.2150C=
ENST00000566510.5:c.*745C=	ENSP00000458139.1:n.*745C=
ENST00000566612.5:c.*319C=	ENSP00000454782.1:n.*319C=
ENST00000611625.4:c.2142C=	ENSP00000481063.1:p.Gly714=
ENST00000612417.4:c.1830+1422C=	ENSP00000478360.1:n.1830+1422C=
ENST00000621016.4:c.1865+1387C=	ENSP00000480664.1:n.1865+1387C=
NM_004360.3:c.2079C= , LRG_301t1:c.2079C=	NP_004351.1:p.Gly693=
XM_011523488.1:c.1344C=	XP_011521790.1:p.Gly448=
XM_011523489.1:c.1344C=	XP_011521791.1:p.Gly448=
NM_001317184.1:c.1896C=	NP_001304113.1:p.Gly632=
NM_001317185.1:c.531C=	NP_001304114.1:p.Gly177=
NM_001317186.1:c.114C=	NP_001304115.1:p.Gly38=
NM_004360.4:c.2079C=	NP_004351.1:p.Gly693=
NM_004360.5:c.2079C= MANE Select	NP_004351.1:p.Gly693=
NM_001317184.2:c.1896C=	NP_001304113.1:p.Gly632=
NM_001317185.2:c.531C=	NP_001304114.1:p.Gly177=
NM_001317186.2:c.114C=	NP_001304115.1:p.Gly38=