Canonical Allele Identifier: CA377089894

Gene: CTNNA3

Linked Data

• MyVariant Identifiers: chr10:g.67726379G>C (hg19) ; chr10:g.65966621G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.65966621G>C , CM000672.2:g.65966621G>C	GRCh38
NC_000010.10:g.67726379G>C , CM000672.1:g.67726379G>C	GRCh37
NC_000010.9:g.67396385G>C	NCBI36
NG_034072.1:g.1734571C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373735.2:n.567C>G
ENST00000682758.1:c.2391C>G	ENSP00000508047.1:p.Ile797Met
ENST00000682945.1:c.2190C>G	ENSP00000506843.1:p.Ile730Met
ENST00000683624.1:c.*1930C>G	ENSP00000507406.1:n.*1930C>G
ENST00000683963.1:c.*1915C>G	ENSP00000507029.1:n.*1915C>G
ENST00000684154.1:c.2391C>G	ENSP00000508371.1:p.Ile797Met
ENST00000433211.7:c.2391C>G MANE Select	ENSP00000389714.1:p.Ile797Met
ENST00000373735.1:n.567C>G
ENST00000433211.6:c.2391C>G	ENSP00000389714.1:p.Ile797Met
NM_001127384.2:c.2391C>G	NP_001120856.1:p.Ile797Met
NM_013266.3:c.2391C>G	NP_037398.2:p.Ile797Met
XM_005269717.2:c.2427C>G	XP_005269774.1:p.Ile809Met
XM_017016151.1:c.2460C>G	XP_016871640.1:p.Ile820Met
XM_017016152.1:c.2616C>G	XP_016871641.1:p.Ile872Met
XM_017016153.1:c.2427C>G	XP_016871642.1:p.Ile809Met
XM_017016154.1:c.1608C>G	XP_016871643.1:p.Ile536Met
XM_017016155.2:c.1608C>G	XP_016871644.1:p.Ile536Met
XM_017016156.1:c.1608C>G	XP_016871645.1:p.Ile536Met
XM_017016157.2:c.1296C>G	XP_016871646.1:p.Ile432Met
NM_013266.4:c.2391C>G MANE Select	NP_037398.2:p.Ile797Met
NM_001127384.3:c.2391C>G	NP_001120856.1:p.Ile797Met