Canonical Allele Identifier: CA2229983173

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823539G= , CM000678.2:g.68823539G=	GRCh38
NC_000016.9:g.68857442G= , CM000678.1:g.68857442G=	GRCh37
NC_000016.8:g.67414943G=	NCBI36
NG_008021.1:g.91248G= , LRG_301:g.91248G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2077G= MANE Select	ENSP00000261769.4:p.Gly693=
ENST00000261769.9:c.2077G=	ENSP00000261769.4:p.Gly693=
ENST00000422392.6:c.1894G=	ENSP00000414946.2:p.Gly632=
ENST00000562118.1:n.295G=
ENST00000562836.5:n.2148G=
ENST00000566510.5:c.*743G=	ENSP00000458139.1:n.*743G=
ENST00000566612.5:c.*317G=	ENSP00000454782.1:n.*317G=
ENST00000611625.4:c.2140G=	ENSP00000481063.1:p.Gly714=
ENST00000612417.4:c.1830+1420G=	ENSP00000478360.1:n.1830+1420G=
ENST00000621016.4:c.1865+1385G=	ENSP00000480664.1:n.1865+1385G=
NM_004360.3:c.2077G= , LRG_301t1:c.2077G=	NP_004351.1:p.Gly693=
XM_011523488.1:c.1342G=	XP_011521790.1:p.Gly448=
XM_011523489.1:c.1342G=	XP_011521791.1:p.Gly448=
NM_001317184.1:c.1894G=	NP_001304113.1:p.Gly632=
NM_001317185.1:c.529G=	NP_001304114.1:p.Gly177=
NM_001317186.1:c.112G=	NP_001304115.1:p.Gly38=
NM_004360.4:c.2077G=	NP_004351.1:p.Gly693=
NM_004360.5:c.2077G= MANE Select	NP_004351.1:p.Gly693=
NM_001317184.2:c.1894G=	NP_001304113.1:p.Gly632=
NM_001317185.2:c.529G=	NP_001304114.1:p.Gly177=
NM_001317186.2:c.112G=	NP_001304115.1:p.Gly38=