Canonical Allele Identifier: CA3200729

Gene: CTNND2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11159734G>A , CM000667.2:g.11159734G>A	GRCh38
NC_000005.9:g.11159846G>A , CM000667.1:g.11159846G>A	GRCh37
NC_000005.8:g.11212846G>A	NCBI36
NG_023544.1:g.749265C>T
NG_023544.2:g.749265C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001332.4:c.2001C>T MANE Select	NP_001323.1:p.Cys667=
ENST00000304623.13:c.2001C>T MANE Select	ENSP00000307134.8:p.Cys667=
NM_001288715.1:c.1728C>T	NP_001275644.1:p.Cys576=
NM_001288716.1:c.990C>T	NP_001275645.1:p.Cys330=
NM_001288717.1:c.702C>T	NP_001275646.1:p.Cys234=
NM_001288717.2:c.702C>T	NP_001275646.1:p.Cys234=
NM_001332.3:c.2001C>T	NP_001323.1:p.Cys667=
NM_001364128.1:c.990C>T	NP_001351057.1:p.Cys330=
NM_001364128.2:c.990C>T	NP_001351057.1:p.Cys330=
NR_109988.1:n.1453C>T
NR_109988.2:n.1856C>T
ENST00000304623.12:c.2001C>T	ENSP00000307134.8:p.Cys667=
ENST00000495388.6:n.1086C>T
ENST00000503622.5:c.990C>T	ENSP00000426887.1:p.Cys330=
ENST00000504499.5:c.*740C>T	ENSP00000421000.1:n.*740C>T
ENST00000511377.5:c.1728C>T	ENSP00000426510.1:p.Cys576=
ENST00000513588.5:c.1263C>T	ENSP00000421093.1:p.Cys421=
ENST00000706271.1:c.990C>T	ENSP00000516315.1:p.Cys330=
ENST00000706272.1:c.1073C>T
XM_005248251.2:c.2001C>T	XP_005248308.1:p.Cys667=
XM_005248251.3:c.2001C>T	XP_005248308.1:p.Cys667=
XM_005248252.1:c.1959C>T	XP_005248309.1:p.Cys653=
XM_005248252.2:c.1959C>T	XP_005248309.1:p.Cys653=
XM_005248253.1:c.1728C>T	XP_005248310.1:p.Cys576=
XM_011513967.1:c.1728C>T	XP_011512269.1:p.Cys576=
XM_011513967.2:c.1728C>T	XP_011512269.1:p.Cys576=
XM_017009072.1:c.1263C>T	XP_016864561.1:p.Cys421=
XM_017009073.1:c.1221C>T	XP_016864562.1:p.Cys407=
XM_017009074.1:c.1263C>T	XP_016864563.1:p.Cys421=
XM_017009075.2:c.990C>T	XP_016864564.1:p.Cys330=
XM_024454368.1:c.330C>T	XP_024310136.1:p.Cys110=