Canonical Allele Identifier: CA2229980615

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822118A= , CM000678.2:g.68822118A=	GRCh38
NC_000016.9:g.68856021A= , CM000678.1:g.68856021A=	GRCh37
NC_000016.8:g.67413522A=	NCBI36
NG_008021.1:g.89827A= , LRG_301:g.89827A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1829A= MANE Select	ENSP00000261769.4:p.Gln610=
ENST00000261769.9:c.1829A=	ENSP00000261769.4:p.Gln610=
ENST00000422392.6:c.1646A=	ENSP00000414946.2:p.Gln549=
ENST00000562836.5:n.1900A=
ENST00000566510.5:c.*495A=	ENSP00000458139.1:n.*495A=
ENST00000566612.5:c.*69A=	ENSP00000454782.1:n.*69A=
ENST00000611625.4:c.1892A=	ENSP00000481063.1:p.Gln631=
ENST00000612417.4:c.1829A=	ENSP00000478360.1:p.Gln610=
ENST00000621016.4:c.1829A=	ENSP00000480664.1:p.Gln610=
NM_004360.3:c.1829A= , LRG_301t1:c.1829A=	NP_004351.1:p.Gln610=
XM_011523488.1:c.1094A=	XP_011521790.1:p.Gln365=
XM_011523489.1:c.1094A=	XP_011521791.1:p.Gln365=
NM_001317184.1:c.1646A=	NP_001304113.1:p.Gln549=
NM_001317185.1:c.281A=	NP_001304114.1:p.Gln94=
NM_001317186.1:c.-137A=	NP_001304115.1:n.-137A=
NM_004360.4:c.1829A=	NP_004351.1:p.Gln610=
NM_004360.5:c.1829A= MANE Select	NP_004351.1:p.Gln610=
NM_001317184.2:c.1646A=	NP_001304113.1:p.Gln549=
NM_001317185.2:c.281A=	NP_001304114.1:p.Gln94=
NM_001317186.2:c.-137A=	NP_001304115.1:n.-137A=