Canonical Allele Identifier: CA2229966855

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810200_68810202delinsTTC , CM000678.2:g.68810200_68810202delinsTTC	GRCh38
NC_000016.9:g.68844103_68844105delinsTTC , CM000678.1:g.68844103_68844105delinsTTC	GRCh37
NC_000016.8:g.67401604_67401606delinsTTC	NCBI36
NG_008021.1:g.77909_77911delinsTTC , LRG_301:g.77909_77911delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.691_693delinsTTC MANE Select	ENSP00000261769.4:p.Phe231=
ENST00000261769.9:c.691_693delinsTTC	ENSP00000261769.4:p.Phe231=
ENST00000422392.6:c.691_693delinsTTC	ENSP00000414946.2:p.Phe231=
ENST00000561751.1:c.454+1352_454+1354delinsTTC
ENST00000562836.5:n.762_764delinsTTC
ENST00000566510.5:c.535_537delinsTTC	ENSP00000458139.1:p.Phe179=
ENST00000566612.5:c.691_693delinsTTC	ENSP00000454782.1:p.Phe231=
ENST00000611625.4:c.691_693delinsTTC	ENSP00000481063.1:p.Phe231=
ENST00000612417.4:c.691_693delinsTTC	ENSP00000478360.1:p.Phe231=
ENST00000621016.4:c.691_693delinsTTC	ENSP00000480664.1:p.Phe231=
NM_004360.3:c.691_693delinsTTC , LRG_301t1:c.691_693delinsTTC	NP_004351.1:p.Phe231=
XM_011523488.1:c.-45_-43delinsTTC	XP_011521790.1:n.-45_-43delinsTTC
XM_011523489.1:c.-45_-43delinsTTC	XP_011521791.1:n.-45_-43delinsTTC
NM_001317184.1:c.691_693delinsTTC	NP_001304113.1:p.Phe231=
NM_001317185.1:c.-925_-923delinsTTC	NP_001304114.1:n.-925_-923delinsTTC
NM_001317186.1:c.-1129_-1127delinsTTC	NP_001304115.1:n.-1129_-1127delinsTTC
NM_004360.4:c.691_693delinsTTC	NP_004351.1:p.Phe231=
NM_004360.5:c.691_693delinsTTC MANE Select	NP_004351.1:p.Phe231=
NM_001317184.2:c.691_693delinsTTC	NP_001304113.1:p.Phe231=
NM_001317185.2:c.-925_-923delinsTTC	NP_001304114.1:n.-925_-923delinsTTC
NM_001317186.2:c.-1129_-1127delinsTTC	NP_001304115.1:n.-1129_-1127delinsTTC