Canonical Allele Identifier: CA2229916564
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738335_68738338delinsCCCT , CM000678.2:g.68738335_68738338delinsCCCT GRCh38
NC_000016.9:g.68772238_68772241delinsCCCT , CM000678.1:g.68772238_68772241delinsCCCT GRCh37
NC_000016.8:g.67329739_67329742delinsCCCT NCBI36
NG_008021.1:g.6044_6047delinsCCCT , LRG_301:g.6044_6047delinsCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.87_90delinsCCCT MANE Select ENSP00000261769.4:p.His29=
ENST00000261769.9:c.87_90delinsCCCT ENSP00000261769.4:p.His29=
ENST00000422392.6:c.87_90delinsCCCT ENSP00000414946.2:p.His29=
ENST00000566510.5:c.87_90delinsCCCT ENSP00000458139.1:p.His29=
ENST00000566612.5:c.87_90delinsCCCT ENSP00000454782.1:p.His29=
ENST00000611625.4:c.87_90delinsCCCT ENSP00000481063.1:p.His29=
ENST00000612417.4:c.87_90delinsCCCT ENSP00000478360.1:p.His29=
ENST00000621016.4:c.87_90delinsCCCT ENSP00000480664.1:p.His29=
NM_004360.3:c.87_90delinsCCCT , LRG_301t1:c.87_90delinsCCCT NP_004351.1:p.His29=
NM_001317184.1:c.87_90delinsCCCT NP_001304113.1:p.His29=
NM_001317185.1:c.-1529_-1526delinsCCCT NP_001304114.1:n.-1529_-1526delinsCCCT
NM_001317186.1:c.-1733_-1730delinsCCCT NP_001304115.1:n.-1733_-1730delinsCCCT
NM_004360.4:c.87_90delinsCCCT NP_004351.1:p.His29=
NM_004360.5:c.87_90delinsCCCT MANE Select NP_004351.1:p.His29=
NM_001317184.2:c.87_90delinsCCCT NP_001304113.1:p.His29=
NM_001317185.2:c.-1529_-1526delinsCCCT NP_001304114.1:n.-1529_-1526delinsCCCT
NM_001317186.2:c.-1733_-1730delinsCCCT NP_001304115.1:n.-1733_-1730delinsCCCT