Canonical Allele Identifier: CA2497098812

Gene: CTNND2

Linked Data

• dbSNP Id: rs1758918641

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385061_11385069del , CM000667.2:g.11385061_11385069del	GRCh38
NC_000005.9:g.11385173_11385181del , CM000667.1:g.11385173_11385181del	GRCh37
NC_000005.8:g.11438173_11438181del	NCBI36
NG_023544.1:g.523933_523941del
NG_023544.2:g.523933_523941del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20176_167-20168del	ENSP00000516315.1:n.167-20176_167-20168del
ENST00000304623.13:c.776_784del MANE Select	ENSP00000307134.8:p.Leu259_Ala261del
ENST00000304623.12:c.776_784del	ENSP00000307134.8:p.Leu259_Ala261del
ENST00000502551.5:c.398-20176_398-20168del	ENSP00000422389.1:n.398-20176_398-20168del
ENST00000503622.5:c.167-20176_167-20168del	ENSP00000426887.1:n.167-20176_167-20168del
ENST00000504354.5:n.217-20176_217-20168del
ENST00000504499.5:c.612+11965_612+11973del	ENSP00000421000.1:n.612+11965_612+11973del
ENST00000511278.5:n.542-20176_542-20168del
ENST00000511377.5:c.503_511del	ENSP00000426510.1:p.Leu168_Ala170del
ENST00000513588.5:c.440-20176_440-20168del	ENSP00000421093.1:n.440-20176_440-20168del
ENST00000513598.5:c.503_511del	ENSP00000426625.1:p.Leu168_Ala170del
ENST00000514132.1:n.425_433del
NM_001288715.1:c.503_511del	NP_001275644.1:p.Leu168_Ala170del
NM_001288716.1:c.167-20176_167-20168del	NP_001275645.1:n.167-20176_167-20168del
NM_001288717.1:c.-123+11965_-123+11973del	NP_001275646.1:n.-123+11965_-123+11973del
NM_001332.3:c.776_784del	NP_001323.1:p.Leu259_Ala261del
NR_109988.1:n.630-20176_630-20168del
XM_005248251.2:c.776_784del	XP_005248308.1:p.Leu259_Ala261del
XM_005248252.1:c.734_742del	XP_005248309.1:p.Leu245_Ala247del
XM_005248253.1:c.503_511del	XP_005248310.1:p.Leu168_Ala170del
XM_011513967.1:c.503_511del	XP_011512269.1:p.Leu168_Ala170del
NM_001364128.1:c.167-20176_167-20168del	NP_001351057.1:n.167-20176_167-20168del
XM_005248251.3:c.776_784del	XP_005248308.1:p.Leu259_Ala261del
XM_005248252.2:c.734_742del	XP_005248309.1:p.Leu245_Ala247del
XM_011513967.2:c.503_511del	XP_011512269.1:p.Leu168_Ala170del
XM_017009072.1:c.440-20176_440-20168del	XP_016864561.1:n.440-20176_440-20168del
XM_017009073.1:c.398-20176_398-20168del	XP_016864562.1:n.398-20176_398-20168del
XM_017009074.1:c.440-20176_440-20168del	XP_016864563.1:n.440-20176_440-20168del
XM_017009075.2:c.167-20176_167-20168del	XP_016864564.1:n.167-20176_167-20168del
NM_001332.4:c.776_784del MANE Select	NP_001323.1:p.Leu259_Ala261del
NM_001288717.2:c.-123+11965_-123+11973del	NP_001275646.1:n.-123+11965_-123+11973del
NR_109988.2:n.1033-20176_1033-20168del
NM_001364128.2:c.167-20176_167-20168del	NP_001351057.1:n.167-20176_167-20168del