Canonical Allele Identifier: CA496152806

Gene: CDH1

Linked Data

• COSMIC: COSM19528
• MyVariant Identifiers: chr16:g.68844199_68844200insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810296dup , CM000678.2:g.68810296dup	GRCh38
NC_000016.9:g.68844199dup , CM000678.1:g.68844199dup	GRCh37
NC_000016.8:g.67401700dup	NCBI36
NG_008021.1:g.78005dup , LRG_301:g.78005dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.787dup MANE Select	ENSP00000261769.4:p.Thr263AsnfsTer6
ENST00000261769.9:c.787dup	ENSP00000261769.4:p.Thr263AsnfsTer6
ENST00000422392.6:c.787dup	ENSP00000414946.2:p.Thr263AsnfsTer6
ENST00000561751.1:c.455-1388dup
ENST00000562836.5:n.858dup
ENST00000566510.5:c.631dup	ENSP00000458139.1:p.Thr211AsnfsTer6
ENST00000566612.5:c.787dup	ENSP00000454782.1:p.Thr263AsnfsTer6
ENST00000611625.4:c.787dup	ENSP00000481063.1:p.Thr263AsnfsTer6
ENST00000612417.4:c.787dup	ENSP00000478360.1:p.Thr263AsnfsTer6
ENST00000621016.4:c.787dup	ENSP00000480664.1:p.Thr263AsnfsTer6
NM_004360.3:c.787dup , LRG_301t1:c.787dup	NP_004351.1:p.Thr263AsnfsTer6
XM_011523488.1:c.52dup	XP_011521790.1:p.Thr18AsnfsTer6
XM_011523489.1:c.52dup	XP_011521791.1:p.Thr18AsnfsTer6
NM_001317184.1:c.787dup	NP_001304113.1:p.Thr263AsnfsTer6
NM_001317185.1:c.-829dup	NP_001304114.1:n.-829dup
NM_001317186.1:c.-1033dup	NP_001304115.1:n.-1033dup
NM_004360.4:c.787dup	NP_004351.1:p.Thr263AsnfsTer6
NM_004360.5:c.787dup MANE Select	NP_004351.1:p.Thr263AsnfsTer6
NM_001317184.2:c.787dup	NP_001304113.1:p.Thr263AsnfsTer6
NM_001317185.2:c.-829dup	NP_001304114.1:n.-829dup
NM_001317186.2:c.-1033dup	NP_001304115.1:n.-1033dup