Canonical Allele Identifier: CA2229958296

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801936C= , CM000678.2:g.68801936C=	GRCh38
NC_000016.9:g.68835839C= , CM000678.1:g.68835839C=	GRCh37
NC_000016.8:g.67393340C=	NCBI36
NG_008021.1:g.69645C= , LRG_301:g.69645C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.387+43C= MANE Select	ENSP00000261769.4:n.387+43C=
ENST00000261769.9:c.387+43C=	ENSP00000261769.4:n.387+43C=
ENST00000422392.6:c.387+43C=	ENSP00000414946.2:n.387+43C=
ENST00000561751.1:c.154+43C=
ENST00000562836.5:n.458+43C=
ENST00000564676.5:n.669+43C=
ENST00000564745.1:n.382+43C=
ENST00000566510.5:c.387+43C=	ENSP00000458139.1:n.387+43C=
ENST00000566612.5:c.387+43C=	ENSP00000454782.1:n.387+43C=
ENST00000611625.4:c.387+43C=	ENSP00000481063.1:n.387+43C=
ENST00000612417.4:c.387+43C=	ENSP00000478360.1:n.387+43C=
ENST00000621016.4:c.387+43C=	ENSP00000480664.1:n.387+43C=
NM_004360.3:c.387+43C= , LRG_301t1:c.387+43C=	NP_004351.1:n.387+43C=
XM_011523488.1:c.-349+43C=	XP_011521790.1:n.-349+43C=
XM_011523489.1:c.-349+43C=	XP_011521791.1:n.-349+43C=
NM_001317184.1:c.387+43C=	NP_001304113.1:n.387+43C=
NM_001317185.1:c.-1229+43C=	NP_001304114.1:n.-1229+43C=
NM_001317186.1:c.-1433+43C=	NP_001304115.1:n.-1433+43C=
NM_004360.4:c.387+43C=	NP_004351.1:n.387+43C=
NM_004360.5:c.387+43C= MANE Select	NP_004351.1:n.387+43C=
NM_001317184.2:c.387+43C=	NP_001304113.1:n.387+43C=
NM_001317185.2:c.-1229+43C=	NP_001304114.1:n.-1229+43C=
NM_001317186.2:c.-1433+43C=	NP_001304115.1:n.-1433+43C=