Canonical Allele Identifier: CA2229980532

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822082G= , CM000678.2:g.68822082G=	GRCh38
NC_000016.9:g.68855985G= , CM000678.1:g.68855985G=	GRCh37
NC_000016.8:g.67413486G=	NCBI36
NG_008021.1:g.89791G= , LRG_301:g.89791G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1793G= MANE Select	ENSP00000261769.4:p.Arg598=
ENST00000261769.9:c.1793G=	ENSP00000261769.4:p.Arg598=
ENST00000422392.6:c.1610G=	ENSP00000414946.2:p.Arg537=
ENST00000562836.5:n.1864G=
ENST00000566510.5:c.*459G=	ENSP00000458139.1:n.*459G=
ENST00000566612.5:c.*33G=	ENSP00000454782.1:n.*33G=
ENST00000611625.4:c.1856G=	ENSP00000481063.1:p.Arg619=
ENST00000612417.4:c.1793G=	ENSP00000478360.1:p.Arg598=
ENST00000621016.4:c.1793G=	ENSP00000480664.1:p.Arg598=
NM_004360.3:c.1793G= , LRG_301t1:c.1793G=	NP_004351.1:p.Arg598=
XM_011523488.1:c.1058G=	XP_011521790.1:p.Arg353=
XM_011523489.1:c.1058G=	XP_011521791.1:p.Arg353=
NM_001317184.1:c.1610G=	NP_001304113.1:p.Arg537=
NM_001317185.1:c.245G=	NP_001304114.1:p.Arg82=
NM_001317186.1:c.-173G=	NP_001304115.1:n.-173G=
NM_004360.4:c.1793G=	NP_004351.1:p.Arg598=
NM_004360.5:c.1793G= MANE Select	NP_004351.1:p.Arg598=
NM_001317184.2:c.1610G=	NP_001304113.1:p.Arg537=
NM_001317185.2:c.245G=	NP_001304114.1:p.Arg82=
NM_001317186.2:c.-173G=	NP_001304115.1:n.-173G=