Canonical Allele Identifier: CA2229916704

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738379G= , CM000678.2:g.68738379G=	GRCh38
NC_000016.9:g.68772282G= , CM000678.1:g.68772282G=	GRCh37
NC_000016.8:g.67329783G=	NCBI36
NG_008021.1:g.6088G= , LRG_301:g.6088G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.131G= MANE Select	ENSP00000261769.4:p.Arg44=
ENST00000261769.9:c.131G=	ENSP00000261769.4:p.Arg44=
ENST00000422392.6:c.131G=	ENSP00000414946.2:p.Arg44=
ENST00000566510.5:c.131G=	ENSP00000458139.1:p.Arg44=
ENST00000566612.5:c.131G=	ENSP00000454782.1:p.Arg44=
ENST00000611625.4:c.131G=	ENSP00000481063.1:p.Arg44=
ENST00000612417.4:c.131G=	ENSP00000478360.1:p.Arg44=
ENST00000621016.4:c.131G=	ENSP00000480664.1:p.Arg44=
NM_004360.3:c.131G= , LRG_301t1:c.131G=	NP_004351.1:p.Arg44=
NM_001317184.1:c.131G=	NP_001304113.1:p.Arg44=
NM_001317185.1:c.-1485G=	NP_001304114.1:n.-1485G=
NM_001317186.1:c.-1689G=	NP_001304115.1:n.-1689G=
NM_004360.4:c.131G=	NP_004351.1:p.Arg44=
NM_004360.5:c.131G= MANE Select	NP_004351.1:p.Arg44=
NM_001317184.2:c.131G=	NP_001304113.1:p.Arg44=
NM_001317185.2:c.-1485G=	NP_001304114.1:n.-1485G=
NM_001317186.2:c.-1689G=	NP_001304115.1:n.-1689G=