Canonical Allele Identifier: CA1916191426

Gene: CTNNA3

Linked Data

• dbSNP Id: rs2078373326

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.65983913G>A , CM000672.2:g.65983913G>A	GRCh38
NC_000010.10:g.67743671G>A , CM000672.1:g.67743671G>A	GRCh37
NC_000010.9:g.67413677G>A	NCBI36
NG_034072.1:g.1717279C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373735.2:n.441+4779C>T
ENST00000682758.1:c.2265+4779C>T	ENSP00000508047.1:n.2265+4779C>T
ENST00000682945.1:c.2064+4779C>T	ENSP00000506843.1:n.2064+4779C>T
ENST00000683624.1:c.*1804+4779C>T	ENSP00000507406.1:n.*1804+4779C>T
ENST00000683963.1:c.*1789+4779C>T	ENSP00000507029.1:n.*1789+4779C>T
ENST00000684154.1:c.2265+4779C>T	ENSP00000508371.1:n.2265+4779C>T
ENST00000433211.7:c.2265+4779C>T MANE Select	ENSP00000389714.1:n.2265+4779C>T
ENST00000373735.1:n.441+4779C>T
ENST00000433211.6:c.2265+4779C>T	ENSP00000389714.1:n.2265+4779C>T
NM_001127384.2:c.2265+4779C>T	NP_001120856.1:n.2265+4779C>T
NM_013266.3:c.2265+4779C>T	NP_037398.2:n.2265+4779C>T
XM_005269717.2:c.2301+4779C>T	XP_005269774.1:n.2301+4779C>T
XM_017016151.1:c.2334+4779C>T	XP_016871640.1:n.2334+4779C>T
XM_017016152.1:c.2490+4779C>T	XP_016871641.1:n.2490+4779C>T
XM_017016153.1:c.2301+4779C>T	XP_016871642.1:n.2301+4779C>T
XM_017016154.1:c.1482+4779C>T	XP_016871643.1:n.1482+4779C>T
XM_017016155.2:c.1482+4779C>T	XP_016871644.1:n.1482+4779C>T
XM_017016156.1:c.1482+4779C>T	XP_016871645.1:n.1482+4779C>T
XM_017016157.2:c.1170+4779C>T	XP_016871646.1:n.1170+4779C>T
NM_013266.4:c.2265+4779C>T MANE Select	NP_037398.2:n.2265+4779C>T
NM_001127384.3:c.2265+4779C>T	NP_001120856.1:n.2265+4779C>T