Canonical Allele Identifier: CA1916354543

Gene: CTNNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.66325548A= , CM000672.2:g.66325548A=	GRCh38
NC_000010.10:g.68085306A= , CM000672.1:g.68085306A=	GRCh37
NC_000010.9:g.67755312A=	NCBI36
NG_034072.1:g.1375644T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682758.1:c.1733-44927T=	ENSP00000508047.1:n.1733-44927T=
ENST00000682945.1:c.1532-44927T=	ENSP00000506843.1:n.1532-44927T=
ENST00000683624.1:c.*1272-44927T=	ENSP00000507406.1:n.*1272-44927T=
ENST00000683963.1:c.*1257-44927T=	ENSP00000507029.1:n.*1257-44927T=
ENST00000684154.1:c.1733-44927T=	ENSP00000508371.1:n.1733-44927T=
ENST00000433211.7:c.1733-44927T= MANE Select	ENSP00000389714.1:n.1733-44927T=
ENST00000433211.6:c.1733-44927T=	ENSP00000389714.1:n.1733-44927T=
NM_001127384.2:c.1733-44927T=	NP_001120856.1:n.1733-44927T=
NM_013266.3:c.1733-44927T=	NP_037398.2:n.1733-44927T=
XM_005269717.2:c.1769-44927T=	XP_005269774.1:n.1769-44927T=
XM_011539721.1:c.1838-44927T=	XP_011538023.1:n.1838-44927T=
XM_011539722.1:c.1838-44927T=	XP_011538024.1:n.1838-44927T=
XM_011539723.1:c.1802-44927T=	XP_011538025.1:n.1802-44927T=
XM_011539724.1:c.1802-44927T=	XP_011538026.1:n.1802-44927T=
XM_011539725.1:c.1802-44927T=	XP_011538027.1:n.1802-44927T=
XM_011539726.1:c.1769-44927T=	XP_011538028.1:n.1769-44927T=
XM_011539727.1:c.1733-44927T=	XP_011538029.1:n.1733-44927T=
XM_017016151.1:c.1802-44927T=	XP_016871640.1:n.1802-44927T=
XM_017016152.1:c.1958-44927T=	XP_016871641.1:n.1958-44927T=
XM_017016153.1:c.1769-44927T=	XP_016871642.1:n.1769-44927T=
XM_017016154.1:c.950-44927T=	XP_016871643.1:n.950-44927T=
XM_017016155.2:c.950-44927T=	XP_016871644.1:n.950-44927T=
XM_017016156.1:c.950-44927T=	XP_016871645.1:n.950-44927T=
XM_017016157.2:c.638-44927T=	XP_016871646.1:n.638-44927T=
NM_013266.4:c.1733-44927T= MANE Select	NP_037398.2:n.1733-44927T=
NM_001127384.3:c.1733-44927T=	NP_001120856.1:n.1733-44927T=