Canonical Allele Identifier: CA2229989705

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68828204G= , CM000678.2:g.68828204G=	GRCh38
NC_000016.9:g.68862107G= , CM000678.1:g.68862107G=	GRCh37
NC_000016.8:g.67419608G=	NCBI36
NG_008021.1:g.95913G= , LRG_301:g.95913G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004360.5:c.2195G= MANE Select	NP_004351.1:p.Arg732=
ENST00000261769.10:c.2195G= MANE Select	ENSP00000261769.4:p.Arg732=
NM_001317184.1:c.2012G=	NP_001304113.1:p.Arg671=
NM_001317184.2:c.2012G=	NP_001304113.1:p.Arg671=
NM_001317185.1:c.647G=	NP_001304114.1:p.Arg216=
NM_001317185.2:c.647G=	NP_001304114.1:p.Arg216=
NM_001317186.1:c.230G=	NP_001304115.1:p.Arg77=
NM_001317186.2:c.230G=	NP_001304115.1:p.Arg77=
NM_004360.3:c.2195G= , LRG_301t1:c.2195G=	NP_004351.1:p.Arg732=
NM_004360.4:c.2195G=	NP_004351.1:p.Arg732=
ENST00000261769.9:c.2195G=	ENSP00000261769.4:p.Arg732=
ENST00000422392.6:c.2012G=	ENSP00000414946.2:p.Arg671=
ENST00000562118.1:n.413G=
ENST00000562836.5:n.2266G=
ENST00000566510.5:c.*861G=	ENSP00000458139.1:n.*861G=
ENST00000566612.5:c.*435G=	ENSP00000454782.1:n.*435G=
ENST00000611625.4:c.2258G=	ENSP00000481063.1:p.Arg753=
ENST00000612417.4:c.1853+1650G=	ENSP00000478360.1:n.1853+1650G=
ENST00000621016.4:c.1866-5999G=	ENSP00000480664.1:n.1866-5999G=
XM_011523488.1:c.1460G=	XP_011521790.1:p.Arg487=
XM_011523489.1:c.1460G=	XP_011521791.1:p.Arg487=