Canonical Allele Identifier: CA2229957879

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801805T= , CM000678.2:g.68801805T=	GRCh38
NC_000016.9:g.68835708T= , CM000678.1:g.68835708T=	GRCh37
NC_000016.8:g.67393209T=	NCBI36
NG_008021.1:g.69514T= , LRG_301:g.69514T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.299T= MANE Select	ENSP00000261769.4:p.Val100=
ENST00000261769.9:c.299T=	ENSP00000261769.4:p.Val100=
ENST00000422392.6:c.299T=	ENSP00000414946.2:p.Val100=
ENST00000561751.1:c.66T=
ENST00000562836.5:n.370T=
ENST00000564676.5:n.581T=
ENST00000564745.1:n.294T=
ENST00000566510.5:c.299T=	ENSP00000458139.1:p.Val100=
ENST00000566612.5:c.299T=	ENSP00000454782.1:p.Val100=
ENST00000611625.4:c.299T=	ENSP00000481063.1:p.Val100=
ENST00000612417.4:c.299T=	ENSP00000478360.1:p.Val100=
ENST00000621016.4:c.299T=	ENSP00000480664.1:p.Val100=
NM_004360.3:c.299T= , LRG_301t1:c.299T=	NP_004351.1:p.Val100=
XM_011523488.1:c.-437T=	XP_011521790.1:n.-437T=
XM_011523489.1:c.-437T=	XP_011521791.1:n.-437T=
NM_001317184.1:c.299T=	NP_001304113.1:p.Val100=
NM_001317185.1:c.-1317T=	NP_001304114.1:n.-1317T=
NM_001317186.1:c.-1521T=	NP_001304115.1:n.-1521T=
NM_004360.4:c.299T=	NP_004351.1:p.Val100=
NM_004360.5:c.299T= MANE Select	NP_004351.1:p.Val100=
NM_001317184.2:c.299T=	NP_001304113.1:p.Val100=
NM_001317185.2:c.-1317T=	NP_001304114.1:n.-1317T=
NM_001317186.2:c.-1521T=	NP_001304115.1:n.-1521T=