Canonical Allele Identifier: CA128217478

Gene: CTNNA1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138925276C>T , CM000667.2:g.138925276C>T	GRCh38
NC_000005.9:g.138260965C>T , CM000667.1:g.138260965C>T	GRCh37
NC_000005.8:g.138288864C>T	NCBI36
NG_047029.1:g.176881C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302763.12:c.1768C>T MANE Select	ENSP00000304669.7:p.Gln590Ter
ENST00000302763.11:c.1768C>T	ENSP00000304669.7:p.Gln590Ter
ENST00000518825.5:c.1768C>T	ENSP00000427821.1:p.Gln590Ter
ENST00000519489.1:n.143C>T
ENST00000521368.5:c.265C>T
ENST00000521387.1:n.202C>T
ENST00000521724.5:c.*1458C>T	ENSP00000431033.1:n.*1458C>T
ENST00000540387.5:c.658C>T	ENSP00000438476.1:p.Gln220Ter
ENST00000627109.2:c.1768C>T	ENSP00000486200.1:p.Gln590Ter
NM_001290307.1:c.1768C>T	NP_001277236.1:p.Gln590Ter
NM_001290309.1:c.1459C>T	NP_001277238.1:p.Gln487Ter
NM_001290310.1:c.1399C>T	NP_001277239.1:p.Gln467Ter
NM_001290312.1:c.658C>T	NP_001277241.1:p.Gln220Ter
NM_001903.3:c.1768C>T	NP_001894.2:p.Gln590Ter
XM_005271899.2:c.658C>T	XP_005271956.1:p.Gln220Ter
XM_006714536.2:c.1768C>T	XP_006714599.1:p.Gln590Ter
XM_011543172.1:c.1768C>T	XP_011541474.1:p.Gln590Ter
NM_001290307.2:c.1768C>T	NP_001277236.1:p.Gln590Ter
NM_001290309.2:c.1459C>T	NP_001277238.1:p.Gln487Ter
NM_001290310.2:c.1399C>T	NP_001277239.1:p.Gln467Ter
NM_001323982.1:c.1768C>T	NP_001310911.1:p.Gln590Ter
NM_001323983.1:c.1768C>T	NP_001310912.1:p.Gln590Ter
NM_001323984.1:c.1768C>T	NP_001310913.1:p.Gln590Ter
NM_001323985.1:c.1768C>T	NP_001310914.1:p.Gln590Ter
NM_001323986.1:c.1675C>T	NP_001310915.1:p.Gln559Ter
NM_001323987.1:c.658C>T	NP_001310916.1:p.Gln220Ter
NM_001323988.1:c.658C>T	NP_001310917.1:p.Gln220Ter
NM_001323989.1:c.658C>T	NP_001310918.1:p.Gln220Ter
NM_001323990.1:c.658C>T	NP_001310919.1:p.Gln220Ter
NM_001323991.1:c.658C>T	NP_001310920.1:p.Gln220Ter
NM_001323992.1:c.658C>T	NP_001310921.1:p.Gln220Ter
NM_001323993.1:c.658C>T	NP_001310922.1:p.Gln220Ter
NM_001323994.1:c.658C>T	NP_001310923.1:p.Gln220Ter
NM_001323995.1:c.658C>T	NP_001310924.1:p.Gln220Ter
NM_001323996.1:c.658C>T	NP_001310925.1:p.Gln220Ter
NM_001323997.1:c.658C>T	NP_001310926.1:p.Gln220Ter
NM_001323998.1:c.658C>T	NP_001310927.1:p.Gln220Ter
NM_001323999.1:c.658C>T	NP_001310928.1:p.Gln220Ter
NM_001324000.1:c.658C>T	NP_001310929.1:p.Gln220Ter
NM_001324001.1:c.658C>T	NP_001310930.1:p.Gln220Ter
NM_001324002.1:c.658C>T	NP_001310931.1:p.Gln220Ter
NM_001324003.1:c.658C>T	NP_001310932.1:p.Gln220Ter
NM_001324004.1:c.658C>T	NP_001310933.1:p.Gln220Ter
NM_001324005.1:c.658C>T	NP_001310934.1:p.Gln220Ter
NM_001324006.1:c.319C>T	NP_001310935.1:p.Gln107Ter
NM_001324007.1:c.319C>T	NP_001310936.1:p.Gln107Ter
NM_001324008.1:c.319C>T	NP_001310937.1:p.Gln107Ter
NM_001324009.1:c.319C>T	NP_001310938.1:p.Gln107Ter
NM_001324010.1:c.319C>T	NP_001310939.1:p.Gln107Ter
NM_001324011.1:c.565C>T	NP_001310940.1:p.Gln189Ter
NM_001324012.1:c.415C>T	NP_001310941.1:p.Gln139Ter
NM_001324013.1:c.415C>T	NP_001310942.1:p.Gln139Ter
NM_001903.4:c.1768C>T	NP_001894.2:p.Gln590Ter
NM_001903.5:c.1768C>T MANE Select	NP_001894.2:p.Gln590Ter
NM_001290309.3:c.1459C>T	NP_001277238.1:p.Gln487Ter
NM_001290310.3:c.1399C>T	NP_001277239.1:p.Gln467Ter
NM_001323982.2:c.1768C>T	NP_001310911.1:p.Gln590Ter
NM_001323984.2:c.1768C>T	NP_001310913.1:p.Gln590Ter
NM_001323985.2:c.1768C>T	NP_001310914.1:p.Gln590Ter
NM_001323986.2:c.1675C>T	NP_001310915.1:p.Gln559Ter
NM_001290307.3:c.1768C>T	NP_001277236.1:p.Gln590Ter