Canonical Allele Identifier: CA2229980847

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822174G= , CM000678.2:g.68822174G=	GRCh38
NC_000016.9:g.68856077G= , CM000678.1:g.68856077G=	GRCh37
NC_000016.8:g.67413578G=	NCBI36
NG_008021.1:g.89883G= , LRG_301:g.89883G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1885G= MANE Select	ENSP00000261769.4:p.Glu629=
ENST00000261769.9:c.1885G=	ENSP00000261769.4:p.Glu629=
ENST00000422392.6:c.1702G=	ENSP00000414946.2:p.Glu568=
ENST00000562836.5:n.1956G=
ENST00000566510.5:c.*551G=	ENSP00000458139.1:n.*551G=
ENST00000566612.5:c.*125G=	ENSP00000454782.1:n.*125G=
ENST00000611625.4:c.1948G=	ENSP00000481063.1:p.Glu650=
ENST00000612417.4:c.1830+55G=	ENSP00000478360.1:n.1830+55G=
ENST00000621016.4:c.1865+20G=	ENSP00000480664.1:n.1865+20G=
NM_004360.3:c.1885G= , LRG_301t1:c.1885G=	NP_004351.1:p.Glu629=
XM_011523488.1:c.1150G=	XP_011521790.1:p.Glu384=
XM_011523489.1:c.1150G=	XP_011521791.1:p.Glu384=
NM_001317184.1:c.1702G=	NP_001304113.1:p.Glu568=
NM_001317185.1:c.337G=	NP_001304114.1:p.Glu113=
NM_001317186.1:c.-81G=	NP_001304115.1:n.-81G=
NM_004360.4:c.1885G=	NP_004351.1:p.Glu629=
NM_004360.5:c.1885G= MANE Select	NP_004351.1:p.Glu629=
NM_001317184.2:c.1702G=	NP_001304113.1:p.Glu568=
NM_001317185.2:c.337G=	NP_001304114.1:p.Glu113=
NM_001317186.2:c.-81G=	NP_001304115.1:n.-81G=