Canonical Allele Identifier: CA2229992142

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829687G= , CM000678.2:g.68829687G=	GRCh38
NC_000016.9:g.68863590G= , CM000678.1:g.68863590G=	GRCh37
NC_000016.8:g.67421091G=	NCBI36
NG_008021.1:g.97396G= , LRG_301:g.97396G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2329G= MANE Select	ENSP00000261769.4:p.Asp777=
ENST00000261769.9:c.2329G=	ENSP00000261769.4:p.Asp777=
ENST00000422392.6:c.2146G=	ENSP00000414946.2:p.Asp716=
ENST00000562118.1:n.547G=
ENST00000562836.5:n.2400G=
ENST00000566510.5:c.*995G=	ENSP00000458139.1:n.*995G=
ENST00000566612.5:c.*569G=	ENSP00000454782.1:n.*569G=
ENST00000611625.4:c.2392G=	ENSP00000481063.1:p.Asp798=
ENST00000612417.4:c.1853+3133G=	ENSP00000478360.1:n.1853+3133G=
ENST00000621016.4:c.1866-4516G=	ENSP00000480664.1:n.1866-4516G=
NM_004360.3:c.2329G= , LRG_301t1:c.2329G=	NP_004351.1:p.Asp777=
XM_011523488.1:c.1594G=	XP_011521790.1:p.Asp532=
XM_011523489.1:c.1594G=	XP_011521791.1:p.Asp532=
NM_001317184.1:c.2146G=	NP_001304113.1:p.Asp716=
NM_001317185.1:c.781G=	NP_001304114.1:p.Asp261=
NM_001317186.1:c.364G=	NP_001304115.1:p.Asp122=
NM_004360.4:c.2329G=	NP_004351.1:p.Asp777=
NM_004360.5:c.2329G= MANE Select	NP_004351.1:p.Asp777=
NM_001317184.2:c.2146G=	NP_001304113.1:p.Asp716=
NM_001317185.2:c.781G=	NP_001304114.1:p.Asp261=
NM_001317186.2:c.364G=	NP_001304115.1:p.Asp122=