Canonical Allele Identifier: CA2229949087

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815670A= , CM000678.2:g.68815670A=	GRCh38
NC_000016.9:g.68849573A= , CM000678.1:g.68849573A=	GRCh37
NC_000016.8:g.67407074A=	NCBI36
NG_008021.1:g.83379A= , LRG_301:g.83379A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1476A= MANE Select	ENSP00000261769.4:p.Arg492=
ENST00000261769.9:c.1476A=	ENSP00000261769.4:p.Arg492=
ENST00000422392.6:c.1293A=	ENSP00000414946.2:p.Arg431=
ENST00000562836.5:n.1547A=
ENST00000566510.5:c.*142A=	ENSP00000458139.1:n.*142A=
ENST00000566612.5:c.1476A=	ENSP00000454782.1:p.Arg492=
ENST00000611625.4:c.1539A=	ENSP00000481063.1:p.Arg513=
ENST00000612417.4:c.1476A=	ENSP00000478360.1:p.Arg492=
ENST00000621016.4:c.1476A=	ENSP00000480664.1:p.Arg492=
NM_004360.3:c.1476A= , LRG_301t1:c.1476A=	NP_004351.1:p.Arg492=
XM_011523488.1:c.741A=	XP_011521790.1:p.Arg247=
XM_011523489.1:c.741A=	XP_011521791.1:p.Arg247=
NM_001317184.1:c.1293A=	NP_001304113.1:p.Arg431=
NM_001317185.1:c.-73A=	NP_001304114.1:n.-73A=
NM_001317186.1:c.-344A=	NP_001304115.1:n.-344A=
NM_004360.4:c.1476A=	NP_004351.1:p.Arg492=
NM_004360.5:c.1476A= MANE Select	NP_004351.1:p.Arg492=
NM_001317184.2:c.1293A=	NP_001304113.1:p.Arg431=
NM_001317185.2:c.-73A=	NP_001304114.1:n.-73A=
NM_001317186.2:c.-344A=	NP_001304115.1:n.-344A=