Canonical Allele Identifier: CA2229915262

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737444_68737453delinsCGCTGCTGCT , CM000678.2:g.68737444_68737453delinsCGCTGCTGCT	GRCh38
NC_000016.9:g.68771347_68771356delinsCGCTGCTGCT , CM000678.1:g.68771347_68771356delinsCGCTGCTGCT	GRCh37
NC_000016.8:g.67328848_67328857delinsCGCTGCTGCT	NCBI36
NG_008021.1:g.5153_5162delinsCGCTGCTGCT , LRG_301:g.5153_5162delinsCGCTGCTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.29_38delinsCGCTGCTGCT MANE Select	ENSP00000261769.4:p.Ala10=
ENST00000261769.9:c.29_38delinsCGCTGCTGCT	ENSP00000261769.4:p.Ala10=
ENST00000422392.6:c.29_38delinsCGCTGCTGCT	ENSP00000414946.2:p.Ala10=
ENST00000566510.5:c.29_38delinsCGCTGCTGCT	ENSP00000458139.1:p.Ala10=
ENST00000566612.5:c.29_38delinsCGCTGCTGCT	ENSP00000454782.1:p.Ala10=
ENST00000611625.4:c.29_38delinsCGCTGCTGCT	ENSP00000481063.1:p.Ala10=
ENST00000612417.4:c.29_38delinsCGCTGCTGCT	ENSP00000478360.1:p.Ala10=
ENST00000621016.4:c.29_38delinsCGCTGCTGCT	ENSP00000480664.1:p.Ala10=
NM_004360.3:c.29_38delinsCGCTGCTGCT , LRG_301t1:c.29_38delinsCGCTGCTGCT	NP_004351.1:p.Ala10=
NM_001317184.1:c.29_38delinsCGCTGCTGCT	NP_001304113.1:p.Ala10=
NM_001317185.1:c.-1587_-1578delinsCGCTGCTGCT	NP_001304114.1:n.-1587_-1578delinsCGCTGCTGCT
NM_001317186.1:c.-1791_-1782delinsCGCTGCTGCT	NP_001304115.1:n.-1791_-1782delinsCGCTGCTGCT
NM_004360.4:c.29_38delinsCGCTGCTGCT	NP_004351.1:p.Ala10=
NM_004360.5:c.29_38delinsCGCTGCTGCT MANE Select	NP_004351.1:p.Ala10=
NM_001317184.2:c.29_38delinsCGCTGCTGCT	NP_001304113.1:p.Ala10=
NM_001317185.2:c.-1587_-1578delinsCGCTGCTGCT	NP_001304114.1:n.-1587_-1578delinsCGCTGCTGCT
NM_001317186.2:c.-1791_-1782delinsCGCTGCTGCT	NP_001304115.1:n.-1791_-1782delinsCGCTGCTGCT