Canonical Allele Identifier: CA361132666

Gene: CTNNA1

Linked Data

• COSMIC: COSM1486327
• MyVariant Identifiers: chr5:g.138264934G>T (hg19) ; chr5:g.138929245G>T (hg38)
• MutSpliceDB: CA361132666

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138929245G>T , CM000667.2:g.138929245G>T	GRCh38
NC_000005.9:g.138264934G>T , CM000667.1:g.138264934G>T	GRCh37
NC_000005.8:g.138292833G>T	NCBI36
NG_047029.1:g.180850G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302763.12:c.1900-1G>T MANE Select	ENSP00000304669.7:n.1900-1G>T
ENST00000302763.11:c.1900-1G>T	ENSP00000304669.7:n.1900-1G>T
ENST00000518825.5:c.1900-1G>T	ENSP00000427821.1:n.1900-1G>T
ENST00000521368.5:c.397-1G>T
ENST00000521387.1:n.334-1G>T
ENST00000521724.5:c.*1590-1G>T	ENSP00000431033.1:n.*1590-1G>T
ENST00000540387.5:c.790-1G>T	ENSP00000438476.1:n.790-1G>T
ENST00000627109.2:c.1900-1G>T	ENSP00000486200.1:n.1900-1G>T
NM_001290307.1:c.1900-1G>T	NP_001277236.1:n.1900-1G>T
NM_001290309.1:c.1591-1G>T	NP_001277238.1:n.1591-1G>T
NM_001290310.1:c.1531-1G>T	NP_001277239.1:n.1531-1G>T
NM_001290312.1:c.790-1G>T	NP_001277241.1:n.790-1G>T
NM_001903.3:c.1900-1G>T	NP_001894.2:n.1900-1G>T
XM_005271899.2:c.790-1G>T	XP_005271956.1:n.790-1G>T
XM_006714536.2:c.1900-1G>T	XP_006714599.1:n.1900-1G>T
XM_011543172.1:c.1900-1G>T	XP_011541474.1:n.1900-1G>T
NM_001290307.2:c.1900-1G>T	NP_001277236.1:n.1900-1G>T
NM_001290309.2:c.1591-1G>T	NP_001277238.1:n.1591-1G>T
NM_001290310.2:c.1531-1G>T	NP_001277239.1:n.1531-1G>T
NM_001323982.1:c.1900-1G>T	NP_001310911.1:n.1900-1G>T
NM_001323983.1:c.1900-1G>T	NP_001310912.1:n.1900-1G>T
NM_001323984.1:c.1900-1G>T	NP_001310913.1:n.1900-1G>T
NM_001323985.1:c.1900-1G>T	NP_001310914.1:n.1900-1G>T
NM_001323986.1:c.1807-1G>T	NP_001310915.1:n.1807-1G>T
NM_001323987.1:c.790-1G>T	NP_001310916.1:n.790-1G>T
NM_001323988.1:c.790-1G>T	NP_001310917.1:n.790-1G>T
NM_001323989.1:c.790-1G>T	NP_001310918.1:n.790-1G>T
NM_001323990.1:c.790-1G>T	NP_001310919.1:n.790-1G>T
NM_001323991.1:c.790-1G>T	NP_001310920.1:n.790-1G>T
NM_001323992.1:c.790-1G>T	NP_001310921.1:n.790-1G>T
NM_001323993.1:c.790-1G>T	NP_001310922.1:n.790-1G>T
NM_001323994.1:c.790-1G>T	NP_001310923.1:n.790-1G>T
NM_001323995.1:c.790-1G>T	NP_001310924.1:n.790-1G>T
NM_001323996.1:c.790-1G>T	NP_001310925.1:n.790-1G>T
NM_001323997.1:c.790-1G>T	NP_001310926.1:n.790-1G>T
NM_001323998.1:c.790-1G>T	NP_001310927.1:n.790-1G>T
NM_001323999.1:c.790-1G>T	NP_001310928.1:n.790-1G>T
NM_001324000.1:c.790-1G>T	NP_001310929.1:n.790-1G>T
NM_001324001.1:c.790-1G>T	NP_001310930.1:n.790-1G>T
NM_001324002.1:c.790-1G>T	NP_001310931.1:n.790-1G>T
NM_001324003.1:c.790-1G>T	NP_001310932.1:n.790-1G>T
NM_001324004.1:c.790-1G>T	NP_001310933.1:n.790-1G>T
NM_001324005.1:c.790-1G>T	NP_001310934.1:n.790-1G>T
NM_001324006.1:c.451-1G>T	NP_001310935.1:n.451-1G>T
NM_001324007.1:c.451-1G>T	NP_001310936.1:n.451-1G>T
NM_001324008.1:c.451-1G>T	NP_001310937.1:n.451-1G>T
NM_001324009.1:c.451-1G>T	NP_001310938.1:n.451-1G>T
NM_001324010.1:c.451-1G>T	NP_001310939.1:n.451-1G>T
NM_001324011.1:c.697-1G>T	NP_001310940.1:n.697-1G>T
NM_001324012.1:c.547-1G>T	NP_001310941.1:n.547-1G>T
NM_001324013.1:c.547-1G>T	NP_001310942.1:n.547-1G>T
NM_001903.4:c.1900-1G>T	NP_001894.2:n.1900-1G>T
NM_001903.5:c.1900-1G>T MANE Select	NP_001894.2:n.1900-1G>T
NM_001290309.3:c.1591-1G>T	NP_001277238.1:n.1591-1G>T
NM_001290310.3:c.1531-1G>T	NP_001277239.1:n.1531-1G>T
NM_001323982.2:c.1900-1G>T	NP_001310911.1:n.1900-1G>T
NM_001323984.2:c.1900-1G>T	NP_001310913.1:n.1900-1G>T
NM_001323985.2:c.1900-1G>T	NP_001310914.1:n.1900-1G>T
NM_001323986.2:c.1807-1G>T	NP_001310915.1:n.1807-1G>T
NM_001290307.3:c.1900-1G>T	NP_001277236.1:n.1900-1G>T