Canonical Allele Identifier: CA667644214

Gene: CTNNA3

Linked Data

• dbSNP Id: rs1189715477
• gnomAD v3: 10-66405536-C-CATTTATAT
• gnomAD v4: 10-66405536-C-CATTTATAT
• MyVariant Identifiers: chr10:g.68165294_68165295insATTTATAT (hg19) ; chr10:g.66405536_66405537insATTTATAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.66405537_66405544dup , CM000672.2:g.66405537_66405544dup	GRCh38
NC_000010.10:g.68165295_68165302dup , CM000672.1:g.68165295_68165302dup	GRCh37
NC_000010.9:g.67835301_67835308dup	NCBI36
NG_034072.1:g.1295648_1295655dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682758.1:c.1532-26192_1532-26185dup	ENSP00000508047.1:n.1532-26192_1532-26185dup
ENST00000682945.1:c.1531+115073_1531+115080dup	ENSP00000506843.1:n.1531+115073_1531+115080dup
ENST00000683624.1:c.*1071-26192_*1071-26185dup	ENSP00000507406.1:n.*1071-26192_*1071-26185dup
ENST00000683963.1:c.*1056-26192_*1056-26185dup	ENSP00000507029.1:n.*1056-26192_*1056-26185dup
ENST00000684154.1:c.1532-26192_1532-26185dup	ENSP00000508371.1:n.1532-26192_1532-26185dup
ENST00000684489.1:n.633-26192_633-26185dup
ENST00000433211.7:c.1532-26192_1532-26185dup MANE Select	ENSP00000389714.1:n.1532-26192_1532-26185dup
ENST00000433211.6:c.1532-26192_1532-26185dup	ENSP00000389714.1:n.1532-26192_1532-26185dup
NM_001127384.2:c.1532-26192_1532-26185dup	NP_001120856.1:n.1532-26192_1532-26185dup
NM_013266.3:c.1532-26192_1532-26185dup	NP_037398.2:n.1532-26192_1532-26185dup
XM_005269717.2:c.1568-26192_1568-26185dup	XP_005269774.1:n.1568-26192_1568-26185dup
XM_011539721.1:c.1637-26192_1637-26185dup	XP_011538023.1:n.1637-26192_1637-26185dup
XM_011539722.1:c.1637-26192_1637-26185dup	XP_011538024.1:n.1637-26192_1637-26185dup
XM_011539723.1:c.1601-26192_1601-26185dup	XP_011538025.1:n.1601-26192_1601-26185dup
XM_011539724.1:c.1601-26192_1601-26185dup	XP_011538026.1:n.1601-26192_1601-26185dup
XM_011539725.1:c.1601-26192_1601-26185dup	XP_011538027.1:n.1601-26192_1601-26185dup
XM_011539726.1:c.1568-26192_1568-26185dup	XP_011538028.1:n.1568-26192_1568-26185dup
XM_011539727.1:c.1532-26192_1532-26185dup	XP_011538029.1:n.1532-26192_1532-26185dup
XM_017016151.1:c.1601-26192_1601-26185dup	XP_016871640.1:n.1601-26192_1601-26185dup
XM_017016152.1:c.1757-26192_1757-26185dup	XP_016871641.1:n.1757-26192_1757-26185dup
XM_017016153.1:c.1568-26192_1568-26185dup	XP_016871642.1:n.1568-26192_1568-26185dup
XM_017016154.1:c.749-26192_749-26185dup	XP_016871643.1:n.749-26192_749-26185dup
XM_017016155.2:c.749-26192_749-26185dup	XP_016871644.1:n.749-26192_749-26185dup
XM_017016156.1:c.749-26192_749-26185dup	XP_016871645.1:n.749-26192_749-26185dup
XM_017016157.2:c.437-26192_437-26185dup	XP_016871646.1:n.437-26192_437-26185dup
NM_013266.4:c.1532-26192_1532-26185dup MANE Select	NP_037398.2:n.1532-26192_1532-26185dup
NM_001127384.3:c.1532-26192_1532-26185dup	NP_001120856.1:n.1532-26192_1532-26185dup