Canonical Allele Identifier: CA1916758543

Gene: CTNNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67175527_67175528delinsGA , CM000672.2:g.67175527_67175528delinsGA	GRCh38
NC_000010.10:g.68935285_68935286delinsGA , CM000672.1:g.68935285_68935286delinsGA	GRCh37
NC_000010.9:g.68605291_68605292delinsGA	NCBI36
NG_034072.1:g.525664_525665delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682166.1:c.*743+4789_*743+4790delinsTC	ENSP00000507319.1:n.*743+4789_*743+4790delinsTC
ENST00000682758.1:c.1047+4789_1047+4790delinsTC	ENSP00000508047.1:n.1047+4789_1047+4790delinsTC
ENST00000682945.1:c.1047+4789_1047+4790delinsTC	ENSP00000506843.1:n.1047+4789_1047+4790delinsTC
ENST00000683272.1:n.1241+4789_1241+4790delinsTC
ENST00000683624.1:c.*743+4789_*743+4790delinsTC	ENSP00000507406.1:n.*743+4789_*743+4790delinsTC
ENST00000683771.1:n.572+4789_572+4790delinsTC
ENST00000683963.1:c.*571+4789_*571+4790delinsTC	ENSP00000507029.1:n.*571+4789_*571+4790delinsTC
ENST00000684154.1:c.1047+4789_1047+4790delinsTC	ENSP00000508371.1:n.1047+4789_1047+4790delinsTC
ENST00000433211.7:c.1047+4789_1047+4790delinsTC MANE Select	ENSP00000389714.1:n.1047+4789_1047+4790delinsTC
ENST00000433211.6:c.1047+4789_1047+4790delinsTC	ENSP00000389714.1:n.1047+4789_1047+4790delinsTC
ENST00000494580.1:c.127+4789_127+4790delinsTC
NM_001127384.2:c.1047+4789_1047+4790delinsTC	NP_001120856.1:n.1047+4789_1047+4790delinsTC
NM_001291133.1:c.*1373_*1374delinsTC	NP_001278062.1:n.*1373_*1374delinsTC
NM_013266.3:c.1047+4789_1047+4790delinsTC	NP_037398.2:n.1047+4789_1047+4790delinsTC
XM_005269717.2:c.1083+4789_1083+4790delinsTC	XP_005269774.1:n.1083+4789_1083+4790delinsTC
XM_011539721.1:c.1152+4789_1152+4790delinsTC	XP_011538023.1:n.1152+4789_1152+4790delinsTC
XM_011539722.1:c.1152+4789_1152+4790delinsTC	XP_011538024.1:n.1152+4789_1152+4790delinsTC
XM_011539723.1:c.1116+4789_1116+4790delinsTC	XP_011538025.1:n.1116+4789_1116+4790delinsTC
XM_011539724.1:c.1116+4789_1116+4790delinsTC	XP_011538026.1:n.1116+4789_1116+4790delinsTC
XM_011539725.1:c.1116+4789_1116+4790delinsTC	XP_011538027.1:n.1116+4789_1116+4790delinsTC
XM_011539726.1:c.1083+4789_1083+4790delinsTC	XP_011538028.1:n.1083+4789_1083+4790delinsTC
XM_011539727.1:c.1047+4789_1047+4790delinsTC	XP_011538029.1:n.1047+4789_1047+4790delinsTC
XM_017016151.1:c.1116+4789_1116+4790delinsTC	XP_016871640.1:n.1116+4789_1116+4790delinsTC
XM_017016152.1:c.1152+4789_1152+4790delinsTC	XP_016871641.1:n.1152+4789_1152+4790delinsTC
XM_017016153.1:c.1083+4789_1083+4790delinsTC	XP_016871642.1:n.1083+4789_1083+4790delinsTC
XM_017016154.1:c.264+4789_264+4790delinsTC	XP_016871643.1:n.264+4789_264+4790delinsTC
XM_017016155.2:c.264+4789_264+4790delinsTC	XP_016871644.1:n.264+4789_264+4790delinsTC
XM_017016156.1:c.264+4789_264+4790delinsTC	XP_016871645.1:n.264+4789_264+4790delinsTC
NM_013266.4:c.1047+4789_1047+4790delinsTC MANE Select	NP_037398.2:n.1047+4789_1047+4790delinsTC
NM_001291133.2:c.*1373_*1374delinsTC	NP_001278062.1:n.*1373_*1374delinsTC
NM_001127384.3:c.1047+4789_1047+4790delinsTC	NP_001120856.1:n.1047+4789_1047+4790delinsTC