Canonical Allele Identifier: CA2229965195

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68808580G= , CM000678.2:g.68808580G=	GRCh38
NC_000016.9:g.68842483G= , CM000678.1:g.68842483G=	GRCh37
NC_000016.8:g.67399984G=	NCBI36
NG_008021.1:g.76289G= , LRG_301:g.76289G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.531+13G= MANE Select	ENSP00000261769.4:n.531+13G=
ENST00000261769.9:c.531+13G=	ENSP00000261769.4:n.531+13G=
ENST00000422392.6:c.531+13G=	ENSP00000414946.2:n.531+13G=
ENST00000561751.1:c.298+13G=
ENST00000562836.5:n.602+13G=
ENST00000564676.5:n.813+13G=
ENST00000564745.1:n.526+13G=
ENST00000566510.5:c.531+13G=	ENSP00000458139.1:n.531+13G=
ENST00000566612.5:c.531+13G=	ENSP00000454782.1:n.531+13G=
ENST00000567320.1:n.41+13G=
ENST00000611625.4:c.531+13G=	ENSP00000481063.1:n.531+13G=
ENST00000612417.4:c.531+13G=	ENSP00000478360.1:n.531+13G=
ENST00000621016.4:c.531+13G=	ENSP00000480664.1:n.531+13G=
NM_004360.3:c.531+13G= , LRG_301t1:c.531+13G=	NP_004351.1:n.531+13G=
XM_011523488.1:c.-205+13G=	XP_011521790.1:n.-205+13G=
XM_011523489.1:c.-205+13G=	XP_011521791.1:n.-205+13G=
NM_001317184.1:c.531+13G=	NP_001304113.1:n.531+13G=
NM_001317185.1:c.-1085+13G=	NP_001304114.1:n.-1085+13G=
NM_001317186.1:c.-1289+13G=	NP_001304115.1:n.-1289+13G=
NM_004360.4:c.531+13G=	NP_004351.1:n.531+13G=
NM_004360.5:c.531+13G= MANE Select	NP_004351.1:n.531+13G=
NM_001317184.2:c.531+13G=	NP_001304113.1:n.531+13G=
NM_001317185.2:c.-1085+13G=	NP_001304114.1:n.-1085+13G=
NM_001317186.2:c.-1289+13G=	NP_001304115.1:n.-1289+13G=