Canonical Allele Identifier: CA2229964886

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68808470_68808472delinsCCT , CM000678.2:g.68808470_68808472delinsCCT	GRCh38
NC_000016.9:g.68842373_68842375delinsCCT , CM000678.1:g.68842373_68842375delinsCCT	GRCh37
NC_000016.8:g.67399874_67399876delinsCCT	NCBI36
NG_008021.1:g.76179_76181delinsCCT , LRG_301:g.76179_76181delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.434_436delinsCCT MANE Select	ENSP00000261769.4:p.Ser145=
ENST00000261769.9:c.434_436delinsCCT	ENSP00000261769.4:p.Ser145=
ENST00000422392.6:c.434_436delinsCCT	ENSP00000414946.2:p.Ser145=
ENST00000561751.1:c.201_203delinsCCT
ENST00000562836.5:n.505_507delinsCCT
ENST00000564676.5:n.716_718delinsCCT
ENST00000564745.1:n.429_431delinsCCT
ENST00000566510.5:c.434_436delinsCCT	ENSP00000458139.1:p.Ser145=
ENST00000566612.5:c.434_436delinsCCT	ENSP00000454782.1:p.Ser145=
ENST00000611625.4:c.434_436delinsCCT	ENSP00000481063.1:p.Ser145=
ENST00000612417.4:c.434_436delinsCCT	ENSP00000478360.1:p.Ser145=
ENST00000621016.4:c.434_436delinsCCT	ENSP00000480664.1:p.Ser145=
NM_004360.3:c.434_436delinsCCT , LRG_301t1:c.434_436delinsCCT	NP_004351.1:p.Ser145=
XM_011523488.1:c.-302_-300delinsCCT	XP_011521790.1:n.-302_-300delinsCCT
XM_011523489.1:c.-302_-300delinsCCT	XP_011521791.1:n.-302_-300delinsCCT
NM_001317184.1:c.434_436delinsCCT	NP_001304113.1:p.Ser145=
NM_001317185.1:c.-1182_-1180delinsCCT	NP_001304114.1:n.-1182_-1180delinsCCT
NM_001317186.1:c.-1386_-1384delinsCCT	NP_001304115.1:n.-1386_-1384delinsCCT
NM_004360.4:c.434_436delinsCCT	NP_004351.1:p.Ser145=
NM_004360.5:c.434_436delinsCCT MANE Select	NP_004351.1:p.Ser145=
NM_001317184.2:c.434_436delinsCCT	NP_001304113.1:p.Ser145=
NM_001317185.2:c.-1182_-1180delinsCCT	NP_001304114.1:n.-1182_-1180delinsCCT
NM_001317186.2:c.-1386_-1384delinsCCT	NP_001304115.1:n.-1386_-1384delinsCCT