Canonical Allele Identifier: CA2580612834
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2503017
ClinVar RCV Id: RCV003229751

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738377_68738420dup , CM000678.2:g.68738377_68738420dup GRCh38
NC_000016.9:g.68772280_68772323dup , CM000678.1:g.68772280_68772323dup GRCh37
NC_000016.8:g.67329781_67329824dup NCBI36
NG_008021.1:g.6086_6129dup , LRG_301:g.6086_6129dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.129_163+9dup
ENST00000261769.9:c.129_163+9dup
ENST00000422392.6:c.129_163+9dup
ENST00000566510.5:c.129_163+9dup
ENST00000566612.5:c.129_163+9dup
ENST00000611625.4:c.129_163+9dup
ENST00000612417.4:c.129_163+9dup
ENST00000621016.4:c.129_163+9dup
NM_004360.3:c.129_163+9dup , LRG_301t1:c.129_163+9dup
NM_001317184.1:c.129_163+9dup
NM_001317185.1:c.-1487_-1453+9dup
NM_001317186.1:c.-1691_-1657+9dup
NM_004360.4:c.129_163+9dup
NM_004360.5:c.129_163+9dup
NM_001317184.2:c.129_163+9dup
NM_001317185.2:c.-1487_-1453+9dup
NM_001317186.2:c.-1691_-1657+9dup