Canonical Allele Identifier: CA2229966930

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810230G= , CM000678.2:g.68810230G=	GRCh38
NC_000016.9:g.68844133G= , CM000678.1:g.68844133G=	GRCh37
NC_000016.8:g.67401634G=	NCBI36
NG_008021.1:g.77939G= , LRG_301:g.77939G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.721G= MANE Select	ENSP00000261769.4:p.Ala241=
ENST00000261769.9:c.721G=	ENSP00000261769.4:p.Ala241=
ENST00000422392.6:c.721G=	ENSP00000414946.2:p.Ala241=
ENST00000561751.1:c.454+1382G=
ENST00000562836.5:n.792G=
ENST00000566510.5:c.565G=	ENSP00000458139.1:p.Ala189=
ENST00000566612.5:c.721G=	ENSP00000454782.1:p.Ala241=
ENST00000611625.4:c.721G=	ENSP00000481063.1:p.Ala241=
ENST00000612417.4:c.721G=	ENSP00000478360.1:p.Ala241=
ENST00000621016.4:c.721G=	ENSP00000480664.1:p.Ala241=
NM_004360.3:c.721G= , LRG_301t1:c.721G=	NP_004351.1:p.Ala241=
XM_011523488.1:c.-15G=	XP_011521790.1:n.-15G=
XM_011523489.1:c.-15G=	XP_011521791.1:n.-15G=
NM_001317184.1:c.721G=	NP_001304113.1:p.Ala241=
NM_001317185.1:c.-895G=	NP_001304114.1:n.-895G=
NM_001317186.1:c.-1099G=	NP_001304115.1:n.-1099G=
NM_004360.4:c.721G=	NP_004351.1:p.Ala241=
NM_004360.5:c.721G= MANE Select	NP_004351.1:p.Ala241=
NM_001317184.2:c.721G=	NP_001304113.1:p.Ala241=
NM_001317185.2:c.-895G=	NP_001304114.1:n.-895G=
NM_001317186.2:c.-1099G=	NP_001304115.1:n.-1099G=