Canonical Allele Identifier: CA114362472

Gene: CTNND2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11110599T>C , CM000667.2:g.11110599T>C	GRCh38
NC_000005.9:g.11110711T>C , CM000667.1:g.11110711T>C	GRCh37
NC_000005.8:g.11163711T>C	NCBI36
NG_023544.1:g.798400A>G
NG_023544.2:g.798400A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.1452+259A>G	ENSP00000516315.1:n.1452+259A>G
ENST00000706272.1:c.1535+259A>G
ENST00000304623.13:c.2463+259A>G MANE Select	ENSP00000307134.8:n.2463+259A>G
ENST00000304623.12:c.2463+259A>G	ENSP00000307134.8:n.2463+259A>G
ENST00000458100.6:c.-251+259A>G	ENSP00000391155.3:n.-251+259A>G
ENST00000495388.6:n.1548+259A>G
ENST00000503622.5:c.1452+259A>G	ENSP00000426887.1:n.1452+259A>G
ENST00000504499.5:c.*1202+259A>G	ENSP00000421000.1:n.*1202+259A>G
ENST00000511377.5:c.2190+259A>G	ENSP00000426510.1:n.2190+259A>G
ENST00000513588.5:c.1725+259A>G	ENSP00000421093.1:n.1725+259A>G
NM_001288715.1:c.2190+259A>G	NP_001275644.1:n.2190+259A>G
NM_001288716.1:c.1452+259A>G	NP_001275645.1:n.1452+259A>G
NM_001288717.1:c.1164+259A>G	NP_001275646.1:n.1164+259A>G
NM_001332.3:c.2463+259A>G	NP_001323.1:n.2463+259A>G
NR_109988.1:n.1915+259A>G
XM_005248251.2:c.2463+259A>G	XP_005248308.1:n.2463+259A>G
XM_005248252.1:c.2421+259A>G	XP_005248309.1:n.2421+259A>G
XM_005248253.1:c.2190+259A>G	XP_005248310.1:n.2190+259A>G
XM_011513967.1:c.2190+259A>G	XP_011512269.1:n.2190+259A>G
NM_001364128.1:c.1452+259A>G	NP_001351057.1:n.1452+259A>G
XM_005248251.3:c.2463+259A>G	XP_005248308.1:n.2463+259A>G
XM_005248252.2:c.2421+259A>G	XP_005248309.1:n.2421+259A>G
XM_011513967.2:c.2190+259A>G	XP_011512269.1:n.2190+259A>G
XM_017009072.1:c.1725+259A>G	XP_016864561.1:n.1725+259A>G
XM_017009073.1:c.1683+259A>G	XP_016864562.1:n.1683+259A>G
XM_017009074.1:c.1725+259A>G	XP_016864563.1:n.1725+259A>G
XM_017009075.2:c.1452+259A>G	XP_016864564.1:n.1452+259A>G
XM_024454368.1:c.792+259A>G	XP_024310136.1:n.792+259A>G
NM_001332.4:c.2463+259A>G MANE Select	NP_001323.1:n.2463+259A>G
NM_001288717.2:c.1164+259A>G	NP_001275646.1:n.1164+259A>G
NR_109988.2:n.2318+259A>G
NM_001364128.2:c.1452+259A>G	NP_001351057.1:n.1452+259A>G