Canonical Allele Identifier: CA1916497126

Gene: CTNNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.66614326G= , CM000672.2:g.66614326G=	GRCh38
NC_000010.10:g.68374084G= , CM000672.1:g.68374084G=	GRCh37
NC_000010.9:g.68044090G=	NCBI36
NG_034072.1:g.1086866C=

Transcript Alleles

HGVS	Amino-acid Change
NM_013266.4:c.1374+7366C= MANE Select	NP_037398.2:n.1374+7366C=
ENST00000433211.7:c.1374+7366C= MANE Select	ENSP00000389714.1:n.1374+7366C=
NM_001127384.2:c.1374+7366C=	NP_001120856.1:n.1374+7366C=
NM_001127384.3:c.1374+7366C=	NP_001120856.1:n.1374+7366C=
NM_013266.3:c.1374+7366C=	NP_037398.2:n.1374+7366C=
ENST00000433211.6:c.1374+7366C=	ENSP00000389714.1:n.1374+7366C=
ENST00000682758.1:c.1374+7366C=	ENSP00000508047.1:n.1374+7366C=
ENST00000682945.1:c.1374+7366C=	ENSP00000506843.1:n.1374+7366C=
ENST00000683272.1:n.1568+7366C=
ENST00000683624.1:c.*1070+7366C=	ENSP00000507406.1:n.*1070+7366C=
ENST00000683963.1:c.*898+7366C=	ENSP00000507029.1:n.*898+7366C=
ENST00000684154.1:c.1374+7366C=	ENSP00000508371.1:n.1374+7366C=
ENST00000684489.1:n.475+7366C=
XM_005269717.2:c.1410+7366C=	XP_005269774.1:n.1410+7366C=
XM_011539721.1:c.1479+7366C=	XP_011538023.1:n.1479+7366C=
XM_011539722.1:c.1479+7366C=	XP_011538024.1:n.1479+7366C=
XM_011539723.1:c.1443+7366C=	XP_011538025.1:n.1443+7366C=
XM_011539724.1:c.1443+7366C=	XP_011538026.1:n.1443+7366C=
XM_011539725.1:c.1443+7366C=	XP_011538027.1:n.1443+7366C=
XM_011539726.1:c.1410+7366C=	XP_011538028.1:n.1410+7366C=
XM_011539727.1:c.1374+7366C=	XP_011538029.1:n.1374+7366C=
XM_017016151.1:c.1443+7366C=	XP_016871640.1:n.1443+7366C=
XM_017016152.1:c.1599+7366C=	XP_016871641.1:n.1599+7366C=
XM_017016153.1:c.1410+7366C=	XP_016871642.1:n.1410+7366C=
XM_017016154.1:c.591+7366C=	XP_016871643.1:n.591+7366C=
XM_017016155.2:c.591+7366C=	XP_016871644.1:n.591+7366C=
XM_017016156.1:c.591+7366C=	XP_016871645.1:n.591+7366C=
XM_017016157.2:c.279+7366C=	XP_016871646.1:n.279+7366C=