Canonical Allele Identifier: CA2229916533

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738329_68738330delinsCT , CM000678.2:g.68738329_68738330delinsCT	GRCh38
NC_000016.9:g.68772232_68772233delinsCT , CM000678.1:g.68772232_68772233delinsCT	GRCh37
NC_000016.8:g.67329733_67329734delinsCT	NCBI36
NG_008021.1:g.6038_6039delinsCT , LRG_301:g.6038_6039delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.81_82delinsCT MANE Select	ENSP00000261769.4:p.Pro27=
ENST00000261769.9:c.81_82delinsCT	ENSP00000261769.4:p.Pro27=
ENST00000422392.6:c.81_82delinsCT	ENSP00000414946.2:p.Pro27=
ENST00000566510.5:c.81_82delinsCT	ENSP00000458139.1:p.Pro27=
ENST00000566612.5:c.81_82delinsCT	ENSP00000454782.1:p.Pro27=
ENST00000611625.4:c.81_82delinsCT	ENSP00000481063.1:p.Pro27=
ENST00000612417.4:c.81_82delinsCT	ENSP00000478360.1:p.Pro27=
ENST00000621016.4:c.81_82delinsCT	ENSP00000480664.1:p.Pro27=
NM_004360.3:c.81_82delinsCT , LRG_301t1:c.81_82delinsCT	NP_004351.1:p.Pro27=
NM_001317184.1:c.81_82delinsCT	NP_001304113.1:p.Pro27=
NM_001317185.1:c.-1535_-1534delinsCT	NP_001304114.1:n.-1535_-1534delinsCT
NM_001317186.1:c.-1739_-1738delinsCT	NP_001304115.1:n.-1739_-1738delinsCT
NM_004360.4:c.81_82delinsCT	NP_004351.1:p.Pro27=
NM_004360.5:c.81_82delinsCT MANE Select	NP_004351.1:p.Pro27=
NM_001317184.2:c.81_82delinsCT	NP_001304113.1:p.Pro27=
NM_001317185.2:c.-1535_-1534delinsCT	NP_001304114.1:n.-1535_-1534delinsCT
NM_001317186.2:c.-1739_-1738delinsCT	NP_001304115.1:n.-1739_-1738delinsCT