Canonical Allele Identifier: CA2229971782

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68780923G= , CM000678.2:g.68780923G=	GRCh38
NC_000016.9:g.68814826G= , CM000678.1:g.68814826G=	GRCh37
NC_000016.8:g.67372327G=	NCBI36
NG_008021.1:g.48632G= , LRG_301:g.48632G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004360.5:c.164-20747G= MANE Select	NP_004351.1:n.164-20747G=
ENST00000261769.10:c.164-20747G= MANE Select	ENSP00000261769.4:n.164-20747G=
NM_001317184.1:c.164-20747G=	NP_001304113.1:n.164-20747G=
NM_001317184.2:c.164-20747G=	NP_001304113.1:n.164-20747G=
NM_001317185.1:c.-1452-20747G=	NP_001304114.1:n.-1452-20747G=
NM_001317185.2:c.-1452-20747G=	NP_001304114.1:n.-1452-20747G=
NM_001317186.1:c.-1656-20747G=	NP_001304115.1:n.-1656-20747G=
NM_001317186.2:c.-1656-20747G=	NP_001304115.1:n.-1656-20747G=
NM_004360.3:c.164-20747G= , LRG_301t1:c.164-20747G=	NP_004351.1:n.164-20747G=
NM_004360.4:c.164-20747G=	NP_004351.1:n.164-20747G=
ENST00000261769.9:c.164-20747G=	ENSP00000261769.4:n.164-20747G=
ENST00000422392.6:c.164-20747G=	ENSP00000414946.2:n.164-20747G=
ENST00000562836.5:n.234+17396G=
ENST00000564676.5:n.445+15359G=
ENST00000564745.1:n.158+9818G=
ENST00000566510.5:c.164-20747G=	ENSP00000458139.1:n.164-20747G=
ENST00000566612.5:c.164-20747G=	ENSP00000454782.1:n.164-20747G=
ENST00000611625.4:c.164-20747G=	ENSP00000481063.1:n.164-20747G=
ENST00000612417.4:c.164-20747G=	ENSP00000478360.1:n.164-20747G=
ENST00000621016.4:c.164-20747G=	ENSP00000480664.1:n.164-20747G=
XM_011523488.1:c.-573+9818G=	XP_011521790.1:n.-573+9818G=
XM_011523489.1:c.-573+15359G=	XP_011521791.1:n.-573+15359G=