Canonical Allele Identifier: CA446595502

Gene: CTNNA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138827655T>C , CM000667.2:g.138827655T>C	GRCh38
NC_000005.9:g.138163344T>C , CM000667.1:g.138163344T>C	GRCh37
NC_000005.8:g.138191243T>C	NCBI36
NG_047029.1:g.79260T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001903.5:c.999T>C MANE Select	NP_001894.2:p.Ile333=
ENST00000302763.12:c.999T>C MANE Select	ENSP00000304669.7:p.Ile333=
NM_001290307.1:c.999T>C	NP_001277236.1:p.Ile333=
NM_001290307.2:c.999T>C	NP_001277236.1:p.Ile333=
NM_001290307.3:c.999T>C	NP_001277236.1:p.Ile333=
NM_001290309.1:c.690T>C	NP_001277238.1:p.Ile230=
NM_001290309.2:c.690T>C	NP_001277238.1:p.Ile230=
NM_001290309.3:c.690T>C	NP_001277238.1:p.Ile230=
NM_001290310.1:c.630T>C	NP_001277239.1:p.Ile210=
NM_001290310.2:c.630T>C	NP_001277239.1:p.Ile210=
NM_001290310.3:c.630T>C	NP_001277239.1:p.Ile210=
NM_001323982.1:c.999T>C	NP_001310911.1:p.Ile333=
NM_001323982.2:c.999T>C	NP_001310911.1:p.Ile333=
NM_001323983.1:c.999T>C	NP_001310912.1:p.Ile333=
NM_001323984.1:c.999T>C	NP_001310913.1:p.Ile333=
NM_001323984.2:c.999T>C	NP_001310913.1:p.Ile333=
NM_001323985.1:c.999T>C	NP_001310914.1:p.Ile333=
NM_001323985.2:c.999T>C	NP_001310914.1:p.Ile333=
NM_001323986.1:c.999T>C	NP_001310915.1:p.Ile333=
NM_001323986.2:c.999T>C	NP_001310915.1:p.Ile333=
NM_001903.3:c.999T>C	NP_001894.2:p.Ile333=
NM_001903.4:c.999T>C	NP_001894.2:p.Ile333=
ENST00000302763.11:c.999T>C	ENSP00000304669.7:p.Ile333=
ENST00000517534.5:n.29T>C
ENST00000518825.5:c.999T>C	ENSP00000427821.1:p.Ile333=
ENST00000521724.5:c.*689T>C	ENSP00000431033.1:n.*689T>C
ENST00000522730.1:n.173T>C
ENST00000523275.5:c.264T>C	ENSP00000429142.1:p.Ile88=
ENST00000627109.2:c.999T>C	ENSP00000486200.1:p.Ile333=
XM_006714536.2:c.999T>C	XP_006714599.1:p.Ile333=
XM_011543172.1:c.999T>C	XP_011541474.1:p.Ile333=