Canonical Allele Identifier: CA208956263

Gene: CTNNA3

Linked Data

• dbSNP Id: rs970128690
• gnomAD v3: 10-65983797-C-G
• gnomAD v4: 10-65983797-C-G
• MyVariant Identifiers: chr10:g.67743555C>G (hg19) ; chr10:g.65983797C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.65983797C>G , CM000672.2:g.65983797C>G	GRCh38
NC_000010.10:g.67743555C>G , CM000672.1:g.67743555C>G	GRCh37
NC_000010.9:g.67413561C>G	NCBI36
NG_034072.1:g.1717395G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373735.2:n.441+4895G>C
ENST00000682758.1:c.2265+4895G>C	ENSP00000508047.1:n.2265+4895G>C
ENST00000682945.1:c.2064+4895G>C	ENSP00000506843.1:n.2064+4895G>C
ENST00000683624.1:c.*1804+4895G>C	ENSP00000507406.1:n.*1804+4895G>C
ENST00000683963.1:c.*1789+4895G>C	ENSP00000507029.1:n.*1789+4895G>C
ENST00000684154.1:c.2265+4895G>C	ENSP00000508371.1:n.2265+4895G>C
ENST00000433211.7:c.2265+4895G>C MANE Select	ENSP00000389714.1:n.2265+4895G>C
ENST00000373735.1:n.441+4895G>C
ENST00000433211.6:c.2265+4895G>C	ENSP00000389714.1:n.2265+4895G>C
NM_001127384.2:c.2265+4895G>C	NP_001120856.1:n.2265+4895G>C
NM_013266.3:c.2265+4895G>C	NP_037398.2:n.2265+4895G>C
XM_005269717.2:c.2301+4895G>C	XP_005269774.1:n.2301+4895G>C
XM_017016151.1:c.2334+4895G>C	XP_016871640.1:n.2334+4895G>C
XM_017016152.1:c.2490+4895G>C	XP_016871641.1:n.2490+4895G>C
XM_017016153.1:c.2301+4895G>C	XP_016871642.1:n.2301+4895G>C
XM_017016154.1:c.1482+4895G>C	XP_016871643.1:n.1482+4895G>C
XM_017016155.2:c.1482+4895G>C	XP_016871644.1:n.1482+4895G>C
XM_017016156.1:c.1482+4895G>C	XP_016871645.1:n.1482+4895G>C
XM_017016157.2:c.1170+4895G>C	XP_016871646.1:n.1170+4895G>C
NM_013266.4:c.2265+4895G>C MANE Select	NP_037398.2:n.2265+4895G>C
NM_001127384.3:c.2265+4895G>C	NP_001120856.1:n.2265+4895G>C