Canonical Allele Identifier: CA2229916603
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738341_68738344delinsCTTT , CM000678.2:g.68738341_68738344delinsCTTT GRCh38
NC_000016.9:g.68772244_68772247delinsCTTT , CM000678.1:g.68772244_68772247delinsCTTT GRCh37
NC_000016.8:g.67329745_67329748delinsCTTT NCBI36
NG_008021.1:g.6050_6053delinsCTTT , LRG_301:g.6050_6053delinsCTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.93_96delinsCTTT MANE Select ENSP00000261769.4:p.Gly31=
ENST00000261769.9:c.93_96delinsCTTT ENSP00000261769.4:p.Gly31=
ENST00000422392.6:c.93_96delinsCTTT ENSP00000414946.2:p.Gly31=
ENST00000566510.5:c.93_96delinsCTTT ENSP00000458139.1:p.Gly31=
ENST00000566612.5:c.93_96delinsCTTT ENSP00000454782.1:p.Gly31=
ENST00000611625.4:c.93_96delinsCTTT ENSP00000481063.1:p.Gly31=
ENST00000612417.4:c.93_96delinsCTTT ENSP00000478360.1:p.Gly31=
ENST00000621016.4:c.93_96delinsCTTT ENSP00000480664.1:p.Gly31=
NM_004360.3:c.93_96delinsCTTT , LRG_301t1:c.93_96delinsCTTT NP_004351.1:p.Gly31=
NM_001317184.1:c.93_96delinsCTTT NP_001304113.1:p.Gly31=
NM_001317185.1:c.-1523_-1520delinsCTTT NP_001304114.1:n.-1523_-1520delinsCTTT
NM_001317186.1:c.-1727_-1724delinsCTTT NP_001304115.1:n.-1727_-1724delinsCTTT
NM_004360.4:c.93_96delinsCTTT NP_004351.1:p.Gly31=
NM_004360.5:c.93_96delinsCTTT MANE Select NP_004351.1:p.Gly31=
NM_001317184.2:c.93_96delinsCTTT NP_001304113.1:p.Gly31=
NM_001317185.2:c.-1523_-1520delinsCTTT NP_001304114.1:n.-1523_-1520delinsCTTT
NM_001317186.2:c.-1727_-1724delinsCTTT NP_001304115.1:n.-1727_-1724delinsCTTT