Canonical Allele Identifier: CA1916160409

Gene: CTNNA3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.65919290A>C , CM000672.2:g.65919290A>C	GRCh38
NC_000010.10:g.67679048A>C , CM000672.1:g.67679048A>C	GRCh37
NC_000010.9:g.67349054A>C	NCBI36
NG_034072.1:g.1781902T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682758.1:c.*1040T>G	ENSP00000508047.1:n.*1040T>G
ENST00000682945.1:c.*1040T>G	ENSP00000506843.1:n.*1040T>G
ENST00000683963.1:c.*3252T>G	ENSP00000507029.1:n.*3252T>G
ENST00000684154.1:c.*1040T>G	ENSP00000508371.1:n.*1040T>G
ENST00000433211.7:c.*1040T>G MANE Select	ENSP00000389714.1:n.*1040T>G
ENST00000433211.6:c.*1040T>G	ENSP00000389714.1:n.*1040T>G
NM_001127384.2:c.*1040T>G	NP_001120856.1:n.*1040T>G
NM_013266.3:c.*1040T>G	NP_037398.2:n.*1040T>G
XM_005269717.2:c.*1040T>G	XP_005269774.1:n.*1040T>G
XM_017016151.1:c.*1040T>G	XP_016871640.1:n.*1040T>G
XM_017016152.1:c.*1040T>G	XP_016871641.1:n.*1040T>G
XM_017016153.1:c.*1040T>G	XP_016871642.1:n.*1040T>G
XM_017016154.1:c.*1040T>G	XP_016871643.1:n.*1040T>G
XM_017016155.2:c.*1040T>G	XP_016871644.1:n.*1040T>G
XM_017016156.1:c.*1040T>G	XP_016871645.1:n.*1040T>G
XM_017016157.2:c.*1040T>G	XP_016871646.1:n.*1040T>G
NM_013266.4:c.*1040T>G MANE Select	NP_037398.2:n.*1040T>G
NM_001127384.3:c.*1040T>G	NP_001120856.1:n.*1040T>G