Canonical Allele Identifier: CA891844132
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801882_68801888dup , CM000678.2:g.68801882_68801888dup GRCh38
NC_000016.9:g.68835785_68835791dup , CM000678.1:g.68835785_68835791dup GRCh37
NC_000016.8:g.67393286_67393292dup NCBI36
NG_008021.1:g.69591_69597dup , LRG_301:g.69591_69597dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.376_382dup MANE Select ENSP00000261769.4:p.His128ProfsTer?
ENST00000261769.9:c.376_382dup ENSP00000261769.4:p.His128ProfsTer?
ENST00000422392.6:c.376_382dup ENSP00000414946.2:p.His128ProfsTer?
ENST00000561751.1:c.143_149dup
ENST00000562836.5:n.447_453dup
ENST00000564676.5:n.658_664dup
ENST00000564745.1:n.371_377dup
ENST00000566510.5:c.376_382dup ENSP00000458139.1:p.His128ProfsTer?
ENST00000566612.5:c.376_382dup ENSP00000454782.1:p.His128ProfsTer?
ENST00000611625.4:c.376_382dup ENSP00000481063.1:p.His128ProfsTer?
ENST00000612417.4:c.376_382dup ENSP00000478360.1:p.His128ProfsTer?
ENST00000621016.4:c.376_382dup ENSP00000480664.1:p.His128ProfsTer?
NM_004360.3:c.376_382dup , LRG_301t1:c.376_382dup NP_004351.1:p.His128ProfsTer?
XM_011523488.1:c.-360_-354dup XP_011521790.1:n.-360_-354dup
XM_011523489.1:c.-360_-354dup XP_011521791.1:n.-360_-354dup
NM_001317184.1:c.376_382dup NP_001304113.1:p.His128ProfsTer?
NM_001317185.1:c.-1240_-1234dup NP_001304114.1:n.-1240_-1234dup
NM_001317186.1:c.-1444_-1438dup NP_001304115.1:n.-1444_-1438dup
NM_004360.4:c.376_382dup NP_004351.1:p.His128ProfsTer?
NM_004360.5:c.376_382dup MANE Select NP_004351.1:p.His128ProfsTer?
NM_001317184.2:c.376_382dup NP_001304113.1:p.His128ProfsTer?
NM_001317185.2:c.-1240_-1234dup NP_001304114.1:n.-1240_-1234dup
NM_001317186.2:c.-1444_-1438dup NP_001304115.1:n.-1444_-1438dup