Canonical Allele Identifier: CA3014580959

Gene: CTNND2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385091_11385092insTGC , CM000667.2:g.11385091_11385092insTGC	GRCh38
NC_000005.9:g.11385203_11385204insTGC , CM000667.1:g.11385203_11385204insTGC	GRCh37
NC_000005.8:g.11438203_11438204insTGC	NCBI36
NG_023544.1:g.523909_523910insAGC
NG_023544.2:g.523909_523910insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20200_167-20199insAGC	ENSP00000516315.1:n.167-20200_167-20199insAGC
ENST00000304623.13:c.752_753insAGC MANE Select	ENSP00000307134.8:p.Ala251_Leu252insAla
ENST00000304623.12:c.752_753insAGC	ENSP00000307134.8:p.Ala251_Leu252insAla
ENST00000502551.5:c.398-20200_398-20199insAGC	ENSP00000422389.1:n.398-20200_398-20199insAGC
ENST00000503622.5:c.167-20200_167-20199insAGC	ENSP00000426887.1:n.167-20200_167-20199insAGC
ENST00000504354.5:n.217-20200_217-20199insAGC
ENST00000504499.5:c.612+11941_612+11942insAGC	ENSP00000421000.1:n.612+11941_612+11942insAGC
ENST00000511278.5:n.542-20200_542-20199insAGC
ENST00000511377.5:c.479_480insAGC	ENSP00000426510.1:p.Ala160_Leu161insAla
ENST00000513588.5:c.440-20200_440-20199insAGC	ENSP00000421093.1:n.440-20200_440-20199insAGC
ENST00000513598.5:c.479_480insAGC	ENSP00000426625.1:p.Ala160_Leu161insAla
ENST00000514132.1:n.401_402insAGC
NM_001288715.1:c.479_480insAGC	NP_001275644.1:p.Ala160_Leu161insAla
NM_001288716.1:c.167-20200_167-20199insAGC	NP_001275645.1:n.167-20200_167-20199insAGC
NM_001288717.1:c.-123+11941_-123+11942insAGC	NP_001275646.1:n.-123+11941_-123+11942insAGC
NM_001332.3:c.752_753insAGC	NP_001323.1:p.Ala251_Leu252insAla
NR_109988.1:n.630-20200_630-20199insAGC
XM_005248251.2:c.752_753insAGC	XP_005248308.1:p.Ala251_Leu252insAla
XM_005248252.1:c.710_711insAGC	XP_005248309.1:p.Ala237_Leu238insAla
XM_005248253.1:c.479_480insAGC	XP_005248310.1:p.Ala160_Leu161insAla
XM_011513967.1:c.479_480insAGC	XP_011512269.1:p.Ala160_Leu161insAla
NM_001364128.1:c.167-20200_167-20199insAGC	NP_001351057.1:n.167-20200_167-20199insAGC
XM_005248251.3:c.752_753insAGC	XP_005248308.1:p.Ala251_Leu252insAla
XM_005248252.2:c.710_711insAGC	XP_005248309.1:p.Ala237_Leu238insAla
XM_011513967.2:c.479_480insAGC	XP_011512269.1:p.Ala160_Leu161insAla
XM_017009072.1:c.440-20200_440-20199insAGC	XP_016864561.1:n.440-20200_440-20199insAGC
XM_017009073.1:c.398-20200_398-20199insAGC	XP_016864562.1:n.398-20200_398-20199insAGC
XM_017009074.1:c.440-20200_440-20199insAGC	XP_016864563.1:n.440-20200_440-20199insAGC
XM_017009075.2:c.167-20200_167-20199insAGC	XP_016864564.1:n.167-20200_167-20199insAGC
NM_001332.4:c.752_753insAGC MANE Select	NP_001323.1:p.Ala251_Leu252insAla
NM_001288717.2:c.-123+11941_-123+11942insAGC	NP_001275646.1:n.-123+11941_-123+11942insAGC
NR_109988.2:n.1033-20200_1033-20199insAGC
NM_001364128.2:c.167-20200_167-20199insAGC	NP_001351057.1:n.167-20200_167-20199insAGC