Canonical Allele Identifier: CA2229980905

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822184A= , CM000678.2:g.68822184A=	GRCh38
NC_000016.9:g.68856087A= , CM000678.1:g.68856087A=	GRCh37
NC_000016.8:g.67413588A=	NCBI36
NG_008021.1:g.89893A= , LRG_301:g.89893A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1895A= MANE Select	ENSP00000261769.4:p.His632=
ENST00000261769.9:c.1895A=	ENSP00000261769.4:p.His632=
ENST00000422392.6:c.1712A=	ENSP00000414946.2:p.His571=
ENST00000562836.5:n.1966A=
ENST00000566510.5:c.*561A=	ENSP00000458139.1:n.*561A=
ENST00000566612.5:c.*135A=	ENSP00000454782.1:n.*135A=
ENST00000611625.4:c.1958A=	ENSP00000481063.1:p.His653=
ENST00000612417.4:c.1830+65A=	ENSP00000478360.1:n.1830+65A=
ENST00000621016.4:c.1865+30A=	ENSP00000480664.1:n.1865+30A=
NM_004360.3:c.1895A= , LRG_301t1:c.1895A=	NP_004351.1:p.His632=
XM_011523488.1:c.1160A=	XP_011521790.1:p.His387=
XM_011523489.1:c.1160A=	XP_011521791.1:p.His387=
NM_001317184.1:c.1712A=	NP_001304113.1:p.His571=
NM_001317185.1:c.347A=	NP_001304114.1:p.His116=
NM_001317186.1:c.-71A=	NP_001304115.1:n.-71A=
NM_004360.4:c.1895A=	NP_004351.1:p.His632=
NM_004360.5:c.1895A= MANE Select	NP_004351.1:p.His632=
NM_001317184.2:c.1712A=	NP_001304113.1:p.His571=
NM_001317185.2:c.347A=	NP_001304114.1:p.His116=
NM_001317186.2:c.-71A=	NP_001304115.1:n.-71A=