Canonical Allele Identifier: CA1916355988

Gene: CTNNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.66328777_66328778delinsCT , CM000672.2:g.66328777_66328778delinsCT	GRCh38
NC_000010.10:g.68088535_68088536delinsCT , CM000672.1:g.68088535_68088536delinsCT	GRCh37
NC_000010.9:g.67758541_67758542delinsCT	NCBI36
NG_034072.1:g.1372414_1372415delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682758.1:c.1733-48157_1733-48156delinsAG	ENSP00000508047.1:n.1733-48157_1733-48156delinsAG
ENST00000682945.1:c.1532-48157_1532-48156delinsAG	ENSP00000506843.1:n.1532-48157_1532-48156delinsAG
ENST00000683624.1:c.*1272-48157_*1272-48156delinsAG	ENSP00000507406.1:n.*1272-48157_*1272-48156delinsAG
ENST00000683963.1:c.*1257-48157_*1257-48156delinsAG	ENSP00000507029.1:n.*1257-48157_*1257-48156delinsAG
ENST00000684154.1:c.1733-48157_1733-48156delinsAG	ENSP00000508371.1:n.1733-48157_1733-48156delinsAG
ENST00000433211.7:c.1733-48157_1733-48156delinsAG MANE Select	ENSP00000389714.1:n.1733-48157_1733-48156delinsAG
ENST00000433211.6:c.1733-48157_1733-48156delinsAG	ENSP00000389714.1:n.1733-48157_1733-48156delinsAG
NM_001127384.2:c.1733-48157_1733-48156delinsAG	NP_001120856.1:n.1733-48157_1733-48156delinsAG
NM_013266.3:c.1733-48157_1733-48156delinsAG	NP_037398.2:n.1733-48157_1733-48156delinsAG
XM_005269717.2:c.1769-48157_1769-48156delinsAG	XP_005269774.1:n.1769-48157_1769-48156delinsAG
XM_011539721.1:c.1838-48157_1838-48156delinsAG	XP_011538023.1:n.1838-48157_1838-48156delinsAG
XM_011539722.1:c.1838-48157_1838-48156delinsAG	XP_011538024.1:n.1838-48157_1838-48156delinsAG
XM_011539723.1:c.1802-48157_1802-48156delinsAG	XP_011538025.1:n.1802-48157_1802-48156delinsAG
XM_011539724.1:c.1802-48157_1802-48156delinsAG	XP_011538026.1:n.1802-48157_1802-48156delinsAG
XM_011539725.1:c.1802-48157_1802-48156delinsAG	XP_011538027.1:n.1802-48157_1802-48156delinsAG
XM_011539726.1:c.1769-48157_1769-48156delinsAG	XP_011538028.1:n.1769-48157_1769-48156delinsAG
XM_011539727.1:c.1733-48157_1733-48156delinsAG	XP_011538029.1:n.1733-48157_1733-48156delinsAG
XM_017016151.1:c.1802-48157_1802-48156delinsAG	XP_016871640.1:n.1802-48157_1802-48156delinsAG
XM_017016152.1:c.1958-48157_1958-48156delinsAG	XP_016871641.1:n.1958-48157_1958-48156delinsAG
XM_017016153.1:c.1769-48157_1769-48156delinsAG	XP_016871642.1:n.1769-48157_1769-48156delinsAG
XM_017016154.1:c.950-48157_950-48156delinsAG	XP_016871643.1:n.950-48157_950-48156delinsAG
XM_017016155.2:c.950-48157_950-48156delinsAG	XP_016871644.1:n.950-48157_950-48156delinsAG
XM_017016156.1:c.950-48157_950-48156delinsAG	XP_016871645.1:n.950-48157_950-48156delinsAG
XM_017016157.2:c.638-48157_638-48156delinsAG	XP_016871646.1:n.638-48157_638-48156delinsAG
NM_013266.4:c.1733-48157_1733-48156delinsAG MANE Select	NP_037398.2:n.1733-48157_1733-48156delinsAG
NM_001127384.3:c.1733-48157_1733-48156delinsAG	NP_001120856.1:n.1733-48157_1733-48156delinsAG