Canonical Allele Identifier: CA2229967159

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810300A= , CM000678.2:g.68810300A=	GRCh38
NC_000016.9:g.68844203A= , CM000678.1:g.68844203A=	GRCh37
NC_000016.8:g.67401704A=	NCBI36
NG_008021.1:g.78009A= , LRG_301:g.78009A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.791A= MANE Select	ENSP00000261769.4:p.Gln264=
ENST00000261769.9:c.791A=	ENSP00000261769.4:p.Gln264=
ENST00000422392.6:c.791A=	ENSP00000414946.2:p.Gln264=
ENST00000561751.1:c.455-1384A=
ENST00000562836.5:n.862A=
ENST00000566510.5:c.635A=	ENSP00000458139.1:p.Gln212=
ENST00000566612.5:c.791A=	ENSP00000454782.1:p.Gln264=
ENST00000611625.4:c.791A=	ENSP00000481063.1:p.Gln264=
ENST00000612417.4:c.791A=	ENSP00000478360.1:p.Gln264=
ENST00000621016.4:c.791A=	ENSP00000480664.1:p.Gln264=
NM_004360.3:c.791A= , LRG_301t1:c.791A=	NP_004351.1:p.Gln264=
XM_011523488.1:c.56A=	XP_011521790.1:p.Gln19=
XM_011523489.1:c.56A=	XP_011521791.1:p.Gln19=
NM_001317184.1:c.791A=	NP_001304113.1:p.Gln264=
NM_001317185.1:c.-825A=	NP_001304114.1:n.-825A=
NM_001317186.1:c.-1029A=	NP_001304115.1:n.-1029A=
NM_004360.4:c.791A=	NP_004351.1:p.Gln264=
NM_004360.5:c.791A= MANE Select	NP_004351.1:p.Gln264=
NM_001317184.2:c.791A=	NP_001304113.1:p.Gln264=
NM_001317185.2:c.-825A=	NP_001304114.1:n.-825A=
NM_001317186.2:c.-1029A=	NP_001304115.1:n.-1029A=