Canonical Allele Identifier: CA2580091958

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1801566
• ClinVar RCV Id: RCV003164600

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833425dup , CM000678.2:g.68833425dup	GRCh38
NC_000016.9:g.68867328dup , CM000678.1:g.68867328dup	GRCh37
NC_000016.8:g.67424829dup	NCBI36
NG_008021.1:g.101134dup , LRG_301:g.101134dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2575dup MANE Select	ENSP00000261769.4:p.Tyr859LeufsTer2
ENST00000261769.9:c.2575dup	ENSP00000261769.4:p.Tyr859LeufsTer2
ENST00000422392.6:c.2392dup	ENSP00000414946.2:p.Tyr798LeufsTer2
ENST00000562118.1:n.793dup
ENST00000562836.5:n.2646dup
ENST00000566510.5:c.*1241dup	ENSP00000458139.1:n.*1241dup
ENST00000566612.5:c.*815dup	ENSP00000454782.1:n.*815dup
ENST00000611625.4:c.2638dup	ENSP00000481063.1:p.Tyr880LeufsTer2
ENST00000612417.4:c.1854-766dup	ENSP00000478360.1:n.1854-766dup
ENST00000621016.4:c.1866-778dup	ENSP00000480664.1:n.1866-778dup
NM_004360.3:c.2575dup , LRG_301t1:c.2575dup	NP_004351.1:p.Tyr859LeufsTer2
XM_011523488.1:c.1840dup	XP_011521790.1:p.Tyr614LeufsTer2
XM_011523489.1:c.1840dup	XP_011521791.1:p.Tyr614LeufsTer2
NM_001317184.1:c.2392dup	NP_001304113.1:p.Tyr798LeufsTer2
NM_001317185.1:c.1027dup	NP_001304114.1:p.Tyr343LeufsTer2
NM_001317186.1:c.610dup	NP_001304115.1:p.Tyr204LeufsTer2
NM_004360.4:c.2575dup	NP_004351.1:p.Tyr859LeufsTer2
NM_004360.5:c.2575dup MANE Select	NP_004351.1:p.Tyr859LeufsTer2
NM_001317184.2:c.2392dup	NP_001304113.1:p.Tyr798LeufsTer2
NM_001317185.2:c.1027dup	NP_001304114.1:p.Tyr343LeufsTer2
NM_001317186.2:c.610dup	NP_001304115.1:p.Tyr204LeufsTer2