Canonical Allele Identifier: CA2229982704

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823440G= , CM000678.2:g.68823440G=	GRCh38
NC_000016.9:g.68857343G= , CM000678.1:g.68857343G=	GRCh37
NC_000016.8:g.67414844G=	NCBI36
NG_008021.1:g.91149G= , LRG_301:g.91149G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1978G= MANE Select	ENSP00000261769.4:p.Val660=
ENST00000261769.9:c.1978G=	ENSP00000261769.4:p.Val660=
ENST00000422392.6:c.1795G=	ENSP00000414946.2:p.Val599=
ENST00000562118.1:n.196G=
ENST00000562836.5:n.2049G=
ENST00000566510.5:c.*644G=	ENSP00000458139.1:n.*644G=
ENST00000566612.5:c.*218G=	ENSP00000454782.1:n.*218G=
ENST00000611625.4:c.2041G=	ENSP00000481063.1:p.Val681=
ENST00000612417.4:c.1830+1321G=	ENSP00000478360.1:n.1830+1321G=
ENST00000621016.4:c.1865+1286G=	ENSP00000480664.1:n.1865+1286G=
NM_004360.3:c.1978G= , LRG_301t1:c.1978G=	NP_004351.1:p.Val660=
XM_011523488.1:c.1243G=	XP_011521790.1:p.Val415=
XM_011523489.1:c.1243G=	XP_011521791.1:p.Val415=
NM_001317184.1:c.1795G=	NP_001304113.1:p.Val599=
NM_001317185.1:c.430G=	NP_001304114.1:p.Val144=
NM_001317186.1:c.13G=	NP_001304115.1:p.Val5=
NM_004360.4:c.1978G=	NP_004351.1:p.Val660=
NM_004360.5:c.1978G= MANE Select	NP_004351.1:p.Val660=
NM_001317184.2:c.1795G=	NP_001304113.1:p.Val599=
NM_001317185.2:c.430G=	NP_001304114.1:p.Val144=
NM_001317186.2:c.13G=	NP_001304115.1:p.Val5=