Canonical Allele Identifier: CA353248

Gene: CTNNA1 CTNNA1-AS1

Linked Data

• ClinVar Variation Id: 223736
• ClinVar RCV Id: RCV000209363
• dbSNP Id: rs869312570
• MyVariant Identifiers: chr5:g.138089522G>A (hg19) ; chr5:g.138753833G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138753833G>A , CM000667.2:g.138753833G>A	GRCh38
NC_000005.9:g.138089522G>A , CM000667.1:g.138089522G>A	GRCh37
NC_000005.8:g.138117421G>A	NCBI36
NG_047029.1:g.5438G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302763.12:c.-3+323G>A (CTNNA1) MANE Select	ENSP00000304669.7:n.-3+323G>A
ENST00000302763.11:c.-3+323G>A (CTNNA1)	ENSP00000304669.7:n.-3+323G>A
ENST00000517980.5:c.-2-28090G>A (CTNNA1)	ENSP00000428439.1:n.-2-28090G>A
ENST00000518910.5:c.-9+323G>A (CTNNA1)	ENSP00000430626.1:n.-9+323G>A
ENST00000519113.5:c.-268G>A (CTNNA1)	ENSP00000430078.1:n.-268G>A
ENST00000519309.5:c.-3+323G>A (CTNNA1)	ENSP00000430671.1:n.-3+323G>A
ENST00000520339.5:c.-473+323G>A (CTNNA1)	ENSP00000428202.1:n.-473+323G>A
ENST00000521724.5:c.-3+323G>A (CTNNA1)	ENSP00000431033.1:n.-3+323G>A
ENST00000521941.1:n.66+323G>A (CTNNA1)
ENST00000522227.5:c.-2-28090G>A (CTNNA1)	ENSP00000429636.1:n.-2-28090G>A
ENST00000523912.5:c.-3+662G>A (CTNNA1)	ENSP00000430304.1:n.-3+662G>A
ENST00000524127.5:c.-2-28090G>A (CTNNA1)	ENSP00000428049.1:n.-2-28090G>A
ENST00000627109.2:c.-3+323G>A (CTNNA1)	ENSP00000486200.1:n.-3+323G>A
NM_001290307.1:c.-3+323G>A (CTNNA1)	NP_001277236.1:n.-3+323G>A
NM_001290309.1:c.-116+323G>A (CTNNA1)	NP_001277238.1:n.-116+323G>A
NM_001290310.1:c.-209+323G>A (CTNNA1)	NP_001277239.1:n.-209+323G>A
NM_001903.3:c.-3+323G>A (CTNNA1)	NP_001894.2:n.-3+323G>A
XM_006714536.2:c.-268G>A (CTNNA1)	XP_006714599.1:n.-268G>A
XM_011543172.1:c.-473+323G>A (CTNNA1)	XP_011541474.1:n.-473+323G>A
XM_011543787.1:c.251C>T (CTNNA1-AS1)	XP_011542089.1:p.Ser84Phe
NM_001290307.2:c.-3+323G>A (CTNNA1)	NP_001277236.1:n.-3+323G>A
NM_001290309.2:c.-116+323G>A (CTNNA1)	NP_001277238.1:n.-116+323G>A
NM_001290310.2:c.-209+323G>A (CTNNA1)	NP_001277239.1:n.-209+323G>A
NM_001323982.1:c.-473+323G>A (CTNNA1)	NP_001310911.1:n.-473+323G>A
NM_001323983.1:c.-268G>A (CTNNA1)	NP_001310912.1:n.-268G>A
NM_001323984.1:c.-21+323G>A (CTNNA1)	NP_001310913.1:n.-21+323G>A
NM_001323985.1:c.-3+323G>A (CTNNA1)	NP_001310914.1:n.-3+323G>A
NM_001323986.1:c.-3+323G>A (CTNNA1)	NP_001310915.1:n.-3+323G>A
NM_001903.4:c.-3+323G>A (CTNNA1)	NP_001894.2:n.-3+323G>A
NR_134244.1:n.92C>T (CTNNA1-AS1)
NM_001903.5:c.-3+323G>A (CTNNA1) MANE Select	NP_001894.2:n.-3+323G>A
NM_001290309.3:c.-116+323G>A (CTNNA1)	NP_001277238.1:n.-116+323G>A
NM_001290310.3:c.-209+323G>A (CTNNA1)	NP_001277239.1:n.-209+323G>A
NM_001323982.2:c.-473+323G>A (CTNNA1)	NP_001310911.1:n.-473+323G>A
NM_001323984.2:c.-21+323G>A (CTNNA1)	NP_001310913.1:n.-21+323G>A
NM_001323985.2:c.-3+323G>A (CTNNA1)	NP_001310914.1:n.-3+323G>A
NM_001323986.2:c.-3+323G>A (CTNNA1)	NP_001310915.1:n.-3+323G>A
NM_001290307.3:c.-3+323G>A (CTNNA1)	NP_001277236.1:n.-3+323G>A