Canonical Allele Identifier: CA2229981026

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822210C= , CM000678.2:g.68822210C=	GRCh38
NC_000016.9:g.68856113C= , CM000678.1:g.68856113C=	GRCh37
NC_000016.8:g.67413614C=	NCBI36
NG_008021.1:g.89919C= , LRG_301:g.89919C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004360.5:c.1921C= MANE Select	NP_004351.1:p.Gln641=
ENST00000261769.10:c.1921C= MANE Select	ENSP00000261769.4:p.Gln641=
NM_001317184.1:c.1738C=	NP_001304113.1:p.Gln580=
NM_001317184.2:c.1738C=	NP_001304113.1:p.Gln580=
NM_001317185.1:c.373C=	NP_001304114.1:p.Gln125=
NM_001317185.2:c.373C=	NP_001304114.1:p.Gln125=
NM_001317186.1:c.-45C=	NP_001304115.1:n.-45C=
NM_001317186.2:c.-45C=	NP_001304115.1:n.-45C=
NM_004360.3:c.1921C= , LRG_301t1:c.1921C=	NP_004351.1:p.Gln641=
NM_004360.4:c.1921C=	NP_004351.1:p.Gln641=
ENST00000261769.9:c.1921C=	ENSP00000261769.4:p.Gln641=
ENST00000422392.6:c.1738C=	ENSP00000414946.2:p.Gln580=
ENST00000562836.5:n.1992C=
ENST00000566510.5:c.*587C=	ENSP00000458139.1:n.*587C=
ENST00000566612.5:c.*161C=	ENSP00000454782.1:n.*161C=
ENST00000611625.4:c.1984C=	ENSP00000481063.1:p.Gln662=
ENST00000612417.4:c.1830+91C=	ENSP00000478360.1:n.1830+91C=
ENST00000621016.4:c.1865+56C=	ENSP00000480664.1:n.1865+56C=
XM_011523488.1:c.1186C=	XP_011521790.1:p.Gln396=
XM_011523489.1:c.1186C=	XP_011521791.1:p.Gln396=