Canonical Allele Identifier: CA915943257

Gene: CTNND2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11236807_11236808insCC , CM000667.2:g.11236807_11236808insCC	GRCh38
NC_000005.9:g.11236919_11236920insCC , CM000667.1:g.11236919_11236920insCC	GRCh37
NC_000005.8:g.11289919_11289920insCC	NCBI36
NG_023544.1:g.672192_672193insGG
NG_023544.2:g.672192_672193insGG

Transcript Alleles

HGVS	Amino-acid Change
NM_001332.4:c.1645_1646insGG MANE Select	NP_001323.1:p.Asp549GlyfsTer8
ENST00000304623.13:c.1645_1646insGG MANE Select	ENSP00000307134.8:p.Asp549GlyfsTer8
NM_001288715.1:c.1372_1373insGG	NP_001275644.1:p.Asp458GlyfsTer8
NM_001288716.1:c.634_635insGG	NP_001275645.1:p.Asp212GlyfsTer8
NM_001288717.1:c.346_347insGG	NP_001275646.1:p.Asp116GlyfsTer8
NM_001288717.2:c.346_347insGG	NP_001275646.1:p.Asp116GlyfsTer8
NM_001332.3:c.1645_1646insGG	NP_001323.1:p.Asp549GlyfsTer8
NM_001364128.1:c.634_635insGG	NP_001351057.1:p.Asp212GlyfsTer8
NM_001364128.2:c.634_635insGG	NP_001351057.1:p.Asp212GlyfsTer8
NR_109988.1:n.1097_1098insGG
NR_109988.2:n.1500_1501insGG
ENST00000304623.12:c.1645_1646insGG	ENSP00000307134.8:p.Asp549GlyfsTer8
ENST00000495388.6:n.730_731insGG
ENST00000503622.5:c.634_635insGG	ENSP00000426887.1:p.Asp212GlyfsTer8
ENST00000504499.5:c.*384_*385insGG	ENSP00000421000.1:n.*384_*385insGG
ENST00000511377.5:c.1372_1373insGG	ENSP00000426510.1:p.Asp458GlyfsTer8
ENST00000513588.5:c.907_908insGG	ENSP00000421093.1:p.Asp303GlyfsTer8
ENST00000706271.1:c.634_635insGG	ENSP00000516315.1:p.Asp212GlyfsTer8
ENST00000706272.1:c.717_718insGG
XM_005248251.2:c.1645_1646insGG	XP_005248308.1:p.Asp549GlyfsTer8
XM_005248251.3:c.1645_1646insGG	XP_005248308.1:p.Asp549GlyfsTer8
XM_005248252.1:c.1603_1604insGG	XP_005248309.1:p.Asp535GlyfsTer8
XM_005248252.2:c.1603_1604insGG	XP_005248309.1:p.Asp535GlyfsTer8
XM_005248253.1:c.1372_1373insGG	XP_005248310.1:p.Asp458GlyfsTer8
XM_011513967.1:c.1372_1373insGG	XP_011512269.1:p.Asp458GlyfsTer8
XM_011513967.2:c.1372_1373insGG	XP_011512269.1:p.Asp458GlyfsTer8
XM_017009072.1:c.907_908insGG	XP_016864561.1:p.Asp303GlyfsTer8
XM_017009073.1:c.865_866insGG	XP_016864562.1:p.Asp289GlyfsTer8
XM_017009074.1:c.907_908insGG	XP_016864563.1:p.Asp303GlyfsTer8
XM_017009075.2:c.634_635insGG	XP_016864564.1:p.Asp212GlyfsTer8
XM_024454368.1:c.-27_-26insGG	XP_024310136.1:n.-27_-26insGG