Canonical Allele Identifier: CA667622512

Gene: CTNNA3

Linked Data

• dbSNP Id: rs10762058
• MyVariant Identifiers: chr10:g.68088508C>A (hg19) ; chr10:g.66328750C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.66328750C>A , CM000672.2:g.66328750C>A	GRCh38
NC_000010.10:g.68088508C>A , CM000672.1:g.68088508C>A	GRCh37
NC_000010.9:g.67758514C>A	NCBI36
NG_034072.1:g.1372442G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682758.1:c.1733-48129G>T	ENSP00000508047.1:n.1733-48129G>T
ENST00000682945.1:c.1532-48129G>T	ENSP00000506843.1:n.1532-48129G>T
ENST00000683624.1:c.*1272-48129G>T	ENSP00000507406.1:n.*1272-48129G>T
ENST00000683963.1:c.*1257-48129G>T	ENSP00000507029.1:n.*1257-48129G>T
ENST00000684154.1:c.1733-48129G>T	ENSP00000508371.1:n.1733-48129G>T
ENST00000433211.7:c.1733-48129G>T MANE Select	ENSP00000389714.1:n.1733-48129G>T
ENST00000433211.6:c.1733-48129G>T	ENSP00000389714.1:n.1733-48129G>T
NM_001127384.2:c.1733-48129G>T	NP_001120856.1:n.1733-48129G>T
NM_013266.3:c.1733-48129G>T	NP_037398.2:n.1733-48129G>T
XM_005269717.2:c.1769-48129G>T	XP_005269774.1:n.1769-48129G>T
XM_011539721.1:c.1838-48129G>T	XP_011538023.1:n.1838-48129G>T
XM_011539722.1:c.1838-48129G>T	XP_011538024.1:n.1838-48129G>T
XM_011539723.1:c.1802-48129G>T	XP_011538025.1:n.1802-48129G>T
XM_011539724.1:c.1802-48129G>T	XP_011538026.1:n.1802-48129G>T
XM_011539725.1:c.1802-48129G>T	XP_011538027.1:n.1802-48129G>T
XM_011539726.1:c.1769-48129G>T	XP_011538028.1:n.1769-48129G>T
XM_011539727.1:c.1733-48129G>T	XP_011538029.1:n.1733-48129G>T
XM_017016151.1:c.1802-48129G>T	XP_016871640.1:n.1802-48129G>T
XM_017016152.1:c.1958-48129G>T	XP_016871641.1:n.1958-48129G>T
XM_017016153.1:c.1769-48129G>T	XP_016871642.1:n.1769-48129G>T
XM_017016154.1:c.950-48129G>T	XP_016871643.1:n.950-48129G>T
XM_017016155.2:c.950-48129G>T	XP_016871644.1:n.950-48129G>T
XM_017016156.1:c.950-48129G>T	XP_016871645.1:n.950-48129G>T
XM_017016157.2:c.638-48129G>T	XP_016871646.1:n.638-48129G>T
NM_013266.4:c.1733-48129G>T MANE Select	NP_037398.2:n.1733-48129G>T
NM_001127384.3:c.1733-48129G>T	NP_001120856.1:n.1733-48129G>T