Canonical Allele Identifier: CA2582342599

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2583714
• ClinVar RCV Id: RCV003334636

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815737dup , CM000678.2:g.68815737dup	GRCh38
NC_000016.9:g.68849640dup , CM000678.1:g.68849640dup	GRCh37
NC_000016.8:g.67407141dup	NCBI36
NG_008021.1:g.83446dup , LRG_301:g.83446dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1543dup MANE Select	ENSP00000261769.4:p.Thr515AsnfsTer22
ENST00000261769.9:c.1543dup	ENSP00000261769.4:p.Thr515AsnfsTer22
ENST00000422392.6:c.1360dup	ENSP00000414946.2:p.Thr454AsnfsTer22
ENST00000562836.5:n.1614dup
ENST00000566510.5:c.*209dup	ENSP00000458139.1:n.*209dup
ENST00000566612.5:c.1543dup	ENSP00000454782.1:p.Thr515AsnfsTer21
ENST00000611625.4:c.1606dup	ENSP00000481063.1:p.Thr536AsnfsTer22
ENST00000612417.4:c.1543dup	ENSP00000478360.1:p.Thr515AsnfsTer22
ENST00000621016.4:c.1543dup	ENSP00000480664.1:p.Thr515AsnfsTer22
NM_004360.3:c.1543dup , LRG_301t1:c.1543dup	NP_004351.1:p.Thr515AsnfsTer22
XM_011523488.1:c.808dup	XP_011521790.1:p.Thr270AsnfsTer22
XM_011523489.1:c.808dup	XP_011521791.1:p.Thr270AsnfsTer22
NM_001317184.1:c.1360dup	NP_001304113.1:p.Thr454AsnfsTer22
NM_001317185.1:c.-6dup	NP_001304114.1:n.-6dup
NM_001317186.1:c.-277dup	NP_001304115.1:n.-277dup
NM_004360.4:c.1543dup	NP_004351.1:p.Thr515AsnfsTer22
NM_004360.5:c.1543dup MANE Select	NP_004351.1:p.Thr515AsnfsTer22
NM_001317184.2:c.1360dup	NP_001304113.1:p.Thr454AsnfsTer22
NM_001317185.2:c.-6dup	NP_001304114.1:n.-6dup
NM_001317186.2:c.-277dup	NP_001304115.1:n.-277dup