Canonical Allele Identifier: CA2229957296

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801707_68801708delinsCT , CM000678.2:g.68801707_68801708delinsCT	GRCh38
NC_000016.9:g.68835610_68835611delinsCT , CM000678.1:g.68835610_68835611delinsCT	GRCh37
NC_000016.8:g.67393111_67393112delinsCT	NCBI36
NG_008021.1:g.69416_69417delinsCT , LRG_301:g.69416_69417delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.201_202delinsCT MANE Select	ENSP00000261769.4:p.Ala67=
ENST00000261769.9:c.201_202delinsCT	ENSP00000261769.4:p.Ala67=
ENST00000422392.6:c.201_202delinsCT	ENSP00000414946.2:p.Ala67=
ENST00000562836.5:n.272_273delinsCT
ENST00000564676.5:n.483_484delinsCT
ENST00000564745.1:n.196_197delinsCT
ENST00000566510.5:c.201_202delinsCT	ENSP00000458139.1:p.Ala67=
ENST00000566612.5:c.201_202delinsCT	ENSP00000454782.1:p.Ala67=
ENST00000611625.4:c.201_202delinsCT	ENSP00000481063.1:p.Ala67=
ENST00000612417.4:c.201_202delinsCT	ENSP00000478360.1:p.Ala67=
ENST00000621016.4:c.201_202delinsCT	ENSP00000480664.1:p.Ala67=
NM_004360.3:c.201_202delinsCT , LRG_301t1:c.201_202delinsCT	NP_004351.1:p.Ala67=
XM_011523488.1:c.-535_-534delinsCT	XP_011521790.1:n.-535_-534delinsCT
XM_011523489.1:c.-535_-534delinsCT	XP_011521791.1:n.-535_-534delinsCT
NM_001317184.1:c.201_202delinsCT	NP_001304113.1:p.Ala67=
NM_001317185.1:c.-1415_-1414delinsCT	NP_001304114.1:n.-1415_-1414delinsCT
NM_001317186.1:c.-1619_-1618delinsCT	NP_001304115.1:n.-1619_-1618delinsCT
NM_004360.4:c.201_202delinsCT	NP_004351.1:p.Ala67=
NM_004360.5:c.201_202delinsCT MANE Select	NP_004351.1:p.Ala67=
NM_001317184.2:c.201_202delinsCT	NP_001304113.1:p.Ala67=
NM_001317185.2:c.-1415_-1414delinsCT	NP_001304114.1:n.-1415_-1414delinsCT
NM_001317186.2:c.-1619_-1618delinsCT	NP_001304115.1:n.-1619_-1618delinsCT