Canonical Allele Identifier: CA1916394922

Gene: CTNNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.66405512_66405513delinsAC , CM000672.2:g.66405512_66405513delinsAC	GRCh38
NC_000010.10:g.68165270_68165271delinsAC , CM000672.1:g.68165270_68165271delinsAC	GRCh37
NC_000010.9:g.67835276_67835277delinsAC	NCBI36
NG_034072.1:g.1295679_1295680delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000682758.1:c.1532-26161_1532-26160delinsGT	ENSP00000508047.1:n.1532-26161_1532-26160delinsGT
ENST00000682945.1:c.1531+115104_1531+115105delinsGT	ENSP00000506843.1:n.1531+115104_1531+115105delinsGT
ENST00000683624.1:c.*1071-26161_*1071-26160delinsGT	ENSP00000507406.1:n.*1071-26161_*1071-26160delinsGT
ENST00000683963.1:c.*1056-26161_*1056-26160delinsGT	ENSP00000507029.1:n.*1056-26161_*1056-26160delinsGT
ENST00000684154.1:c.1532-26161_1532-26160delinsGT	ENSP00000508371.1:n.1532-26161_1532-26160delinsGT
ENST00000684489.1:n.633-26161_633-26160delinsGT
ENST00000433211.7:c.1532-26161_1532-26160delinsGT MANE Select	ENSP00000389714.1:n.1532-26161_1532-26160delinsGT
ENST00000433211.6:c.1532-26161_1532-26160delinsGT	ENSP00000389714.1:n.1532-26161_1532-26160delinsGT
NM_001127384.2:c.1532-26161_1532-26160delinsGT	NP_001120856.1:n.1532-26161_1532-26160delinsGT
NM_013266.3:c.1532-26161_1532-26160delinsGT	NP_037398.2:n.1532-26161_1532-26160delinsGT
XM_005269717.2:c.1568-26161_1568-26160delinsGT	XP_005269774.1:n.1568-26161_1568-26160delinsGT
XM_011539721.1:c.1637-26161_1637-26160delinsGT	XP_011538023.1:n.1637-26161_1637-26160delinsGT
XM_011539722.1:c.1637-26161_1637-26160delinsGT	XP_011538024.1:n.1637-26161_1637-26160delinsGT
XM_011539723.1:c.1601-26161_1601-26160delinsGT	XP_011538025.1:n.1601-26161_1601-26160delinsGT
XM_011539724.1:c.1601-26161_1601-26160delinsGT	XP_011538026.1:n.1601-26161_1601-26160delinsGT
XM_011539725.1:c.1601-26161_1601-26160delinsGT	XP_011538027.1:n.1601-26161_1601-26160delinsGT
XM_011539726.1:c.1568-26161_1568-26160delinsGT	XP_011538028.1:n.1568-26161_1568-26160delinsGT
XM_011539727.1:c.1532-26161_1532-26160delinsGT	XP_011538029.1:n.1532-26161_1532-26160delinsGT
XM_017016151.1:c.1601-26161_1601-26160delinsGT	XP_016871640.1:n.1601-26161_1601-26160delinsGT
XM_017016152.1:c.1757-26161_1757-26160delinsGT	XP_016871641.1:n.1757-26161_1757-26160delinsGT
XM_017016153.1:c.1568-26161_1568-26160delinsGT	XP_016871642.1:n.1568-26161_1568-26160delinsGT
XM_017016154.1:c.749-26161_749-26160delinsGT	XP_016871643.1:n.749-26161_749-26160delinsGT
XM_017016155.2:c.749-26161_749-26160delinsGT	XP_016871644.1:n.749-26161_749-26160delinsGT
XM_017016156.1:c.749-26161_749-26160delinsGT	XP_016871645.1:n.749-26161_749-26160delinsGT
XM_017016157.2:c.437-26161_437-26160delinsGT	XP_016871646.1:n.437-26161_437-26160delinsGT
NM_013266.4:c.1532-26161_1532-26160delinsGT MANE Select	NP_037398.2:n.1532-26161_1532-26160delinsGT
NM_001127384.3:c.1532-26161_1532-26160delinsGT	NP_001120856.1:n.1532-26161_1532-26160delinsGT