Canonical Allele Identifier: CA2229992035

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829666A= , CM000678.2:g.68829666A=	GRCh38
NC_000016.9:g.68863569A= , CM000678.1:g.68863569A=	GRCh37
NC_000016.8:g.67421070A=	NCBI36
NG_008021.1:g.97375A= , LRG_301:g.97375A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2308A= MANE Select	ENSP00000261769.4:p.Ser770=
ENST00000261769.9:c.2308A=	ENSP00000261769.4:p.Ser770=
ENST00000422392.6:c.2125A=	ENSP00000414946.2:p.Ser709=
ENST00000562118.1:n.526A=
ENST00000562836.5:n.2379A=
ENST00000566510.5:c.*974A=	ENSP00000458139.1:n.*974A=
ENST00000566612.5:c.*548A=	ENSP00000454782.1:n.*548A=
ENST00000611625.4:c.2371A=	ENSP00000481063.1:p.Ser791=
ENST00000612417.4:c.1853+3112A=	ENSP00000478360.1:n.1853+3112A=
ENST00000621016.4:c.1866-4537A=	ENSP00000480664.1:n.1866-4537A=
NM_004360.3:c.2308A= , LRG_301t1:c.2308A=	NP_004351.1:p.Ser770=
XM_011523488.1:c.1573A=	XP_011521790.1:p.Ser525=
XM_011523489.1:c.1573A=	XP_011521791.1:p.Ser525=
NM_001317184.1:c.2125A=	NP_001304113.1:p.Ser709=
NM_001317185.1:c.760A=	NP_001304114.1:p.Ser254=
NM_001317186.1:c.343A=	NP_001304115.1:p.Ser115=
NM_004360.4:c.2308A=	NP_004351.1:p.Ser770=
NM_004360.5:c.2308A= MANE Select	NP_004351.1:p.Ser770=
NM_001317184.2:c.2125A=	NP_001304113.1:p.Ser709=
NM_001317185.2:c.760A=	NP_001304114.1:p.Ser254=
NM_001317186.2:c.343A=	NP_001304115.1:p.Ser115=