Canonical Allele Identifier: CA1916394839

Gene: CTNNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.66405316G= , CM000672.2:g.66405316G=	GRCh38
NC_000010.10:g.68165074G= , CM000672.1:g.68165074G=	GRCh37
NC_000010.9:g.67835080G=	NCBI36
NG_034072.1:g.1295876C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682758.1:c.1532-25964C=	ENSP00000508047.1:n.1532-25964C=
ENST00000682945.1:c.1531+115301C=	ENSP00000506843.1:n.1531+115301C=
ENST00000683624.1:c.*1071-25964C=	ENSP00000507406.1:n.*1071-25964C=
ENST00000683963.1:c.*1056-25964C=	ENSP00000507029.1:n.*1056-25964C=
ENST00000684154.1:c.1532-25964C=	ENSP00000508371.1:n.1532-25964C=
ENST00000684489.1:n.633-25964C=
ENST00000433211.7:c.1532-25964C= MANE Select	ENSP00000389714.1:n.1532-25964C=
ENST00000433211.6:c.1532-25964C=	ENSP00000389714.1:n.1532-25964C=
NM_001127384.2:c.1532-25964C=	NP_001120856.1:n.1532-25964C=
NM_013266.3:c.1532-25964C=	NP_037398.2:n.1532-25964C=
XM_005269717.2:c.1568-25964C=	XP_005269774.1:n.1568-25964C=
XM_011539721.1:c.1637-25964C=	XP_011538023.1:n.1637-25964C=
XM_011539722.1:c.1637-25964C=	XP_011538024.1:n.1637-25964C=
XM_011539723.1:c.1601-25964C=	XP_011538025.1:n.1601-25964C=
XM_011539724.1:c.1601-25964C=	XP_011538026.1:n.1601-25964C=
XM_011539725.1:c.1601-25964C=	XP_011538027.1:n.1601-25964C=
XM_011539726.1:c.1568-25964C=	XP_011538028.1:n.1568-25964C=
XM_011539727.1:c.1532-25964C=	XP_011538029.1:n.1532-25964C=
XM_017016151.1:c.1601-25964C=	XP_016871640.1:n.1601-25964C=
XM_017016152.1:c.1757-25964C=	XP_016871641.1:n.1757-25964C=
XM_017016153.1:c.1568-25964C=	XP_016871642.1:n.1568-25964C=
XM_017016154.1:c.749-25964C=	XP_016871643.1:n.749-25964C=
XM_017016155.2:c.749-25964C=	XP_016871644.1:n.749-25964C=
XM_017016156.1:c.749-25964C=	XP_016871645.1:n.749-25964C=
XM_017016157.2:c.437-25964C=	XP_016871646.1:n.437-25964C=
NM_013266.4:c.1532-25964C= MANE Select	NP_037398.2:n.1532-25964C=
NM_001127384.3:c.1532-25964C=	NP_001120856.1:n.1532-25964C=