Canonical Allele Identifier: CA2229978323
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819687C= , CM000678.2:g.68819687C= GRCh38
NC_000016.9:g.68853590C= , CM000678.1:g.68853590C= GRCh37
NC_000016.8:g.67411091C= NCBI36
NG_008021.1:g.87396C= , LRG_301:g.87396C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1711+262C= MANE Select ENSP00000261769.4:n.1711+262C=
ENST00000261769.9:c.1711+262C= ENSP00000261769.4:n.1711+262C=
ENST00000422392.6:c.1528+262C= ENSP00000414946.2:n.1528+262C=
ENST00000562836.5:n.1782+262C=
ENST00000566510.5:c.*377+262C= ENSP00000458139.1:n.*377+262C=
ENST00000566612.5:c.1566-2314C= ENSP00000454782.1:n.1566-2314C=
ENST00000611625.4:c.1774+262C= ENSP00000481063.1:n.1774+262C=
ENST00000612417.4:c.1711+262C= ENSP00000478360.1:n.1711+262C=
ENST00000621016.4:c.1711+262C= ENSP00000480664.1:n.1711+262C=
NM_004360.3:c.1711+262C= , LRG_301t1:c.1711+262C= NP_004351.1:n.1711+262C=
XM_011523488.1:c.976+262C= XP_011521790.1:n.976+262C=
XM_011523489.1:c.976+262C= XP_011521791.1:n.976+262C=
NM_001317184.1:c.1528+262C= NP_001304113.1:n.1528+262C=
NM_001317185.1:c.163+262C= NP_001304114.1:n.163+262C=
NM_001317186.1:c.-254-2314C= NP_001304115.1:n.-254-2314C=
NM_004360.4:c.1711+262C= NP_004351.1:n.1711+262C=
NM_004360.5:c.1711+262C= MANE Select NP_004351.1:n.1711+262C=
NM_001317184.2:c.1528+262C= NP_001304113.1:n.1528+262C=
NM_001317185.2:c.163+262C= NP_001304114.1:n.163+262C=
NM_001317186.2:c.-254-2314C= NP_001304115.1:n.-254-2314C=