Canonical Allele Identifier: CA209006434

Gene: CTNNA3

Linked Data

• dbSNP Id: rs919915256
• gnomAD v2: 10-68165186-A-G
• gnomAD v3: 10-66405428-A-G
• gnomAD v4: 10-66405428-A-G
• MyVariant Identifiers: chr10:g.68165186A>G (hg19) ; chr10:g.66405428A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.66405428A>G , CM000672.2:g.66405428A>G	GRCh38
NC_000010.10:g.68165186A>G , CM000672.1:g.68165186A>G	GRCh37
NC_000010.9:g.67835192A>G	NCBI36
NG_034072.1:g.1295764T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682758.1:c.1532-26076T>C	ENSP00000508047.1:n.1532-26076T>C
ENST00000682945.1:c.1531+115189T>C	ENSP00000506843.1:n.1531+115189T>C
ENST00000683624.1:c.*1071-26076T>C	ENSP00000507406.1:n.*1071-26076T>C
ENST00000683963.1:c.*1056-26076T>C	ENSP00000507029.1:n.*1056-26076T>C
ENST00000684154.1:c.1532-26076T>C	ENSP00000508371.1:n.1532-26076T>C
ENST00000684489.1:n.633-26076T>C
ENST00000433211.7:c.1532-26076T>C MANE Select	ENSP00000389714.1:n.1532-26076T>C
ENST00000433211.6:c.1532-26076T>C	ENSP00000389714.1:n.1532-26076T>C
NM_001127384.2:c.1532-26076T>C	NP_001120856.1:n.1532-26076T>C
NM_013266.3:c.1532-26076T>C	NP_037398.2:n.1532-26076T>C
XM_005269717.2:c.1568-26076T>C	XP_005269774.1:n.1568-26076T>C
XM_011539721.1:c.1637-26076T>C	XP_011538023.1:n.1637-26076T>C
XM_011539722.1:c.1637-26076T>C	XP_011538024.1:n.1637-26076T>C
XM_011539723.1:c.1601-26076T>C	XP_011538025.1:n.1601-26076T>C
XM_011539724.1:c.1601-26076T>C	XP_011538026.1:n.1601-26076T>C
XM_011539725.1:c.1601-26076T>C	XP_011538027.1:n.1601-26076T>C
XM_011539726.1:c.1568-26076T>C	XP_011538028.1:n.1568-26076T>C
XM_011539727.1:c.1532-26076T>C	XP_011538029.1:n.1532-26076T>C
XM_017016151.1:c.1601-26076T>C	XP_016871640.1:n.1601-26076T>C
XM_017016152.1:c.1757-26076T>C	XP_016871641.1:n.1757-26076T>C
XM_017016153.1:c.1568-26076T>C	XP_016871642.1:n.1568-26076T>C
XM_017016154.1:c.749-26076T>C	XP_016871643.1:n.749-26076T>C
XM_017016155.2:c.749-26076T>C	XP_016871644.1:n.749-26076T>C
XM_017016156.1:c.749-26076T>C	XP_016871645.1:n.749-26076T>C
XM_017016157.2:c.437-26076T>C	XP_016871646.1:n.437-26076T>C
NM_013266.4:c.1532-26076T>C MANE Select	NP_037398.2:n.1532-26076T>C
NM_001127384.3:c.1532-26076T>C	NP_001120856.1:n.1532-26076T>C