Canonical Allele Identifier: CA361122971

Gene: CTNNA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138810088T>G , CM000667.2:g.138810088T>G	GRCh38
NC_000005.9:g.138145777T>G , CM000667.1:g.138145777T>G	GRCh37
NC_000005.8:g.138173676T>G	NCBI36
NG_047029.1:g.61693T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001903.5:c.352T>G MANE Select	NP_001894.2:p.Ser118Ala
ENST00000302763.12:c.352T>G MANE Select	ENSP00000304669.7:p.Ser118Ala
NM_001290307.1:c.352T>G	NP_001277236.1:p.Ser118Ala
NM_001290307.2:c.352T>G	NP_001277236.1:p.Ser118Ala
NM_001290307.3:c.352T>G	NP_001277236.1:p.Ser118Ala
NM_001290309.1:c.43T>G	NP_001277238.1:p.Ser15Ala
NM_001290309.2:c.43T>G	NP_001277238.1:p.Ser15Ala
NM_001290309.3:c.43T>G	NP_001277238.1:p.Ser15Ala
NM_001290310.1:c.-5-13T>G	NP_001277239.1:n.-5-13T>G
NM_001290310.2:c.-5-13T>G	NP_001277239.1:n.-5-13T>G
NM_001290310.3:c.-5-13T>G	NP_001277239.1:n.-5-13T>G
NM_001323982.1:c.352T>G	NP_001310911.1:p.Ser118Ala
NM_001323982.2:c.352T>G	NP_001310911.1:p.Ser118Ala
NM_001323983.1:c.352T>G	NP_001310912.1:p.Ser118Ala
NM_001323984.1:c.352T>G	NP_001310913.1:p.Ser118Ala
NM_001323984.2:c.352T>G	NP_001310913.1:p.Ser118Ala
NM_001323985.1:c.352T>G	NP_001310914.1:p.Ser118Ala
NM_001323985.2:c.352T>G	NP_001310914.1:p.Ser118Ala
NM_001323986.1:c.352T>G	NP_001310915.1:p.Ser118Ala
NM_001323986.2:c.352T>G	NP_001310915.1:p.Ser118Ala
NM_001903.3:c.352T>G	NP_001894.2:p.Ser118Ala
NM_001903.4:c.352T>G	NP_001894.2:p.Ser118Ala
ENST00000302763.11:c.352T>G	ENSP00000304669.7:p.Ser118Ala
ENST00000517980.5:c.352T>G
ENST00000518585.1:n.169T>G
ENST00000518825.5:c.352T>G	ENSP00000427821.1:p.Ser118Ala
ENST00000518910.5:c.43T>G	ENSP00000430626.1:p.Ser15Ala
ENST00000519113.5:c.352T>G	ENSP00000430078.1:p.Ser118Ala
ENST00000519309.5:c.*298T>G	ENSP00000430671.1:n.*298T>G
ENST00000520158.5:c.352T>G	ENSP00000429457.1:p.Ser118Ala
ENST00000521724.5:c.*42T>G	ENSP00000431033.1:n.*42T>G
ENST00000522227.5:c.352T>G	ENSP00000429636.1:p.Ser118Ala
ENST00000523912.5:c.352T>G	ENSP00000430304.1:p.Ser118Ala
ENST00000627109.2:c.352T>G	ENSP00000486200.1:p.Ser118Ala
XM_006714536.2:c.352T>G	XP_006714599.1:p.Ser118Ala
XM_011543172.1:c.352T>G	XP_011541474.1:p.Ser118Ala