Canonical Allele Identifier: CA2229990319

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68828323G= , CM000678.2:g.68828323G=	GRCh38
NC_000016.9:g.68862226G= , CM000678.1:g.68862226G=	GRCh37
NC_000016.8:g.67419727G=	NCBI36
NG_008021.1:g.96032G= , LRG_301:g.96032G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2295+19G= MANE Select	ENSP00000261769.4:n.2295+19G=
ENST00000261769.9:c.2295+19G=	ENSP00000261769.4:n.2295+19G=
ENST00000422392.6:c.2112+19G=	ENSP00000414946.2:n.2112+19G=
ENST00000562118.1:n.513+19G=
ENST00000562836.5:n.2366+19G=
ENST00000566510.5:c.*961+19G=	ENSP00000458139.1:n.*961+19G=
ENST00000566612.5:c.*535+19G=	ENSP00000454782.1:n.*535+19G=
ENST00000611625.4:c.2358+19G=	ENSP00000481063.1:n.2358+19G=
ENST00000612417.4:c.1853+1769G=	ENSP00000478360.1:n.1853+1769G=
ENST00000621016.4:c.1866-5880G=	ENSP00000480664.1:n.1866-5880G=
NM_004360.3:c.2295+19G= , LRG_301t1:c.2295+19G=	NP_004351.1:n.2295+19G=
XM_011523488.1:c.1560+19G=	XP_011521790.1:n.1560+19G=
XM_011523489.1:c.1560+19G=	XP_011521791.1:n.1560+19G=
NM_001317184.1:c.2112+19G=	NP_001304113.1:n.2112+19G=
NM_001317185.1:c.747+19G=	NP_001304114.1:n.747+19G=
NM_001317186.1:c.330+19G=	NP_001304115.1:n.330+19G=
NM_004360.4:c.2295+19G=	NP_004351.1:n.2295+19G=
NM_004360.5:c.2295+19G= MANE Select	NP_004351.1:n.2295+19G=
NM_001317184.2:c.2112+19G=	NP_001304113.1:n.2112+19G=
NM_001317185.2:c.747+19G=	NP_001304114.1:n.747+19G=
NM_001317186.2:c.330+19G=	NP_001304115.1:n.330+19G=