Canonical Allele Identifier: CA2229978114

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833301G= , CM000678.2:g.68833301G=	GRCh38
NC_000016.9:g.68867204G= , CM000678.1:g.68867204G=	GRCh37
NC_000016.8:g.67424705G=	NCBI36
NG_008021.1:g.101010G= , LRG_301:g.101010G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2451G= MANE Select	ENSP00000261769.4:p.Ala817=
ENST00000261769.9:c.2451G=	ENSP00000261769.4:p.Ala817=
ENST00000422392.6:c.2268G=	ENSP00000414946.2:p.Ala756=
ENST00000562118.1:n.669G=
ENST00000562836.5:n.2522G=
ENST00000566510.5:c.*1117G=	ENSP00000458139.1:n.*1117G=
ENST00000566612.5:c.*691G=	ENSP00000454782.1:n.*691G=
ENST00000611625.4:c.2514G=	ENSP00000481063.1:p.Ala838=
ENST00000612417.4:c.1854-890G=	ENSP00000478360.1:n.1854-890G=
ENST00000621016.4:c.1866-902G=	ENSP00000480664.1:n.1866-902G=
NM_004360.3:c.2451G= , LRG_301t1:c.2451G=	NP_004351.1:p.Ala817=
XM_011523488.1:c.1716G=	XP_011521790.1:p.Ala572=
XM_011523489.1:c.1716G=	XP_011521791.1:p.Ala572=
NM_001317184.1:c.2268G=	NP_001304113.1:p.Ala756=
NM_001317185.1:c.903G=	NP_001304114.1:p.Ala301=
NM_001317186.1:c.486G=	NP_001304115.1:p.Ala162=
NM_004360.4:c.2451G=	NP_004351.1:p.Ala817=
NM_004360.5:c.2451G= MANE Select	NP_004351.1:p.Ala817=
NM_001317184.2:c.2268G=	NP_001304113.1:p.Ala756=
NM_001317185.2:c.903G=	NP_001304114.1:p.Ala301=
NM_001317186.2:c.486G=	NP_001304115.1:p.Ala162=