Canonical Allele Identifier: CA667644186

Gene: CTNNA3

Linked Data

• dbSNP Id: rs1227591332
• MyVariant Identifiers: chr10:g.68165233_68165234insATTTTTTTTTTTAAGA (hg19) ; chr10:g.66405475_66405476insATTTTTTTTTTTAAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.66405475_66405476insATTTTTTTTTTTAAGA , CM000672.2:g.66405475_66405476insATTTTTTTTTTTAAGA	GRCh38
NC_000010.10:g.68165233_68165234insATTTTTTTTTTTAAGA , CM000672.1:g.68165233_68165234insATTTTTTTTTTTAAGA	GRCh37
NC_000010.9:g.67835239_67835240insATTTTTTTTTTTAAGA	NCBI36
NG_034072.1:g.1295716_1295717insTCTTAAAAAAAAAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682758.1:c.1532-26124_1532-26123insTCTTAAAAAAAAAAAT	ENSP00000508047.1:n.1532-26124_1532-26123insTCTTAAAAAAAAAAAT
ENST00000682945.1:c.1531+115141_1531+115142insTCTTAAAAAAAAAAAT	ENSP00000506843.1:n.1531+115141_1531+115142insTCTTAAAAAAAAAAA...
ENST00000683624.1:c.*1071-26124_*1071-26123insTCTTAAAAAAAAAAAT	ENSP00000507406.1:n.*1071-26124_*1071-26123insTCTTAAAAAAAAAAA...
ENST00000683963.1:c.*1056-26124_*1056-26123insTCTTAAAAAAAAAAAT	ENSP00000507029.1:n.*1056-26124_*1056-26123insTCTTAAAAAAAAAAA...
ENST00000684154.1:c.1532-26124_1532-26123insTCTTAAAAAAAAAAAT	ENSP00000508371.1:n.1532-26124_1532-26123insTCTTAAAAAAAAAAAT
ENST00000684489.1:n.633-26124_633-26123insTCTTAAAAAAAAAAAT
ENST00000433211.7:c.1532-26124_1532-26123insTCTTAAAAAAAAAAAT MANE Select	ENSP00000389714.1:n.1532-26124_1532-26123insTCTTAAAAAAAAAAAT
ENST00000433211.6:c.1532-26124_1532-26123insTCTTAAAAAAAAAAAT	ENSP00000389714.1:n.1532-26124_1532-26123insTCTTAAAAAAAAAAAT
NM_001127384.2:c.1532-26124_1532-26123insTCTTAAAAAAAAAAAT	NP_001120856.1:n.1532-26124_1532-26123insTCTTAAAAAAAAAAAT
NM_013266.3:c.1532-26124_1532-26123insTCTTAAAAAAAAAAAT	NP_037398.2:n.1532-26124_1532-26123insTCTTAAAAAAAAAAAT
XM_005269717.2:c.1568-26124_1568-26123insTCTTAAAAAAAAAAAT	XP_005269774.1:n.1568-26124_1568-26123insTCTTAAAAAAAAAAAT
XM_011539721.1:c.1637-26124_1637-26123insTCTTAAAAAAAAAAAT	XP_011538023.1:n.1637-26124_1637-26123insTCTTAAAAAAAAAAAT
XM_011539722.1:c.1637-26124_1637-26123insTCTTAAAAAAAAAAAT	XP_011538024.1:n.1637-26124_1637-26123insTCTTAAAAAAAAAAAT
XM_011539723.1:c.1601-26124_1601-26123insTCTTAAAAAAAAAAAT	XP_011538025.1:n.1601-26124_1601-26123insTCTTAAAAAAAAAAAT
XM_011539724.1:c.1601-26124_1601-26123insTCTTAAAAAAAAAAAT	XP_011538026.1:n.1601-26124_1601-26123insTCTTAAAAAAAAAAAT
XM_011539725.1:c.1601-26124_1601-26123insTCTTAAAAAAAAAAAT	XP_011538027.1:n.1601-26124_1601-26123insTCTTAAAAAAAAAAAT
XM_011539726.1:c.1568-26124_1568-26123insTCTTAAAAAAAAAAAT	XP_011538028.1:n.1568-26124_1568-26123insTCTTAAAAAAAAAAAT
XM_011539727.1:c.1532-26124_1532-26123insTCTTAAAAAAAAAAAT	XP_011538029.1:n.1532-26124_1532-26123insTCTTAAAAAAAAAAAT
XM_017016151.1:c.1601-26124_1601-26123insTCTTAAAAAAAAAAAT	XP_016871640.1:n.1601-26124_1601-26123insTCTTAAAAAAAAAAAT
XM_017016152.1:c.1757-26124_1757-26123insTCTTAAAAAAAAAAAT	XP_016871641.1:n.1757-26124_1757-26123insTCTTAAAAAAAAAAAT
XM_017016153.1:c.1568-26124_1568-26123insTCTTAAAAAAAAAAAT	XP_016871642.1:n.1568-26124_1568-26123insTCTTAAAAAAAAAAAT
XM_017016154.1:c.749-26124_749-26123insTCTTAAAAAAAAAAAT	XP_016871643.1:n.749-26124_749-26123insTCTTAAAAAAAAAAAT
XM_017016155.2:c.749-26124_749-26123insTCTTAAAAAAAAAAAT	XP_016871644.1:n.749-26124_749-26123insTCTTAAAAAAAAAAAT
XM_017016156.1:c.749-26124_749-26123insTCTTAAAAAAAAAAAT	XP_016871645.1:n.749-26124_749-26123insTCTTAAAAAAAAAAAT
XM_017016157.2:c.437-26124_437-26123insTCTTAAAAAAAAAAAT	XP_016871646.1:n.437-26124_437-26123insTCTTAAAAAAAAAAAT
NM_013266.4:c.1532-26124_1532-26123insTCTTAAAAAAAAAAAT MANE Select	NP_037398.2:n.1532-26124_1532-26123insTCTTAAAAAAAAAAAT
NM_001127384.3:c.1532-26124_1532-26123insTCTTAAAAAAAAAAAT	NP_001120856.1:n.1532-26124_1532-26123insTCTTAAAAAAAAAAAT