Canonical Allele Identifier: CA2160960586

Gene: AKT1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104770815C= , CM000676.2:g.104770815C=	GRCh38
NC_000014.8:g.105237152C= , CM000676.1:g.105237152C=	GRCh37
NC_000014.7:g.104308197C=	NCBI36
NG_012188.1:g.29930G= , LRG_721:g.29930G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554192.6:c.1194G=	ENSP00000450681.3:p.Ser398=
ENST00000554585.6:c.*119G=	ENSP00000481526.2:n.*119G=
ENST00000555458.6:c.1293G=	ENSP00000451470.3:p.Ser431=
ENST00000553797.2:c.1368G=	ENSP00000507566.1:p.Ser456=
ENST00000554826.2:n.1762G=
ENST00000610370.2:n.3279G=
ENST00000683058.1:n.1170G=
ENST00000683722.1:c.1293G=	ENSP00000507879.1:p.Ser431=
ENST00000684058.1:n.850G=
ENST00000407796.7:c.1293G=	ENSP00000384293.2:p.Ser431=
ENST00000649815.2:c.1293G= MANE Select	ENSP00000497822.1:p.Ser431=
ENST00000349310.7:c.1293G=	ENSP00000270202.4:p.Ser431=
ENST00000402615.6:c.1293G=	ENSP00000385326.2:p.Ser431=
ENST00000407796.6:c.1293G=	ENSP00000384293.2:p.Ser431=
ENST00000544168.5:n.1228G=
ENST00000553506.5:n.1691G=
ENST00000554192.5:c.403G=
ENST00000554581.5:c.1293G=	ENSP00000451828.1:p.Ser431=
ENST00000554585.5:c.560G=	ENSP00000481526.1:n.560G=
ENST00000554848.5:c.1293G=	ENSP00000451166.1:p.Ser431=
ENST00000555458.5:c.400G=
ENST00000555528.5:c.1293G=	ENSP00000450688.1:p.Ser431=
ENST00000557552.1:n.7257G=
ENST00000610370.1:n.1724G=
NM_001014431.1:c.1293G=	NP_001014431.1:p.Ser431=
NM_001014432.1:c.1293G= , LRG_721t1:c.1293G=	NP_001014432.1:p.Ser431=
NM_005163.2:c.1293G= , LRG_721t2:c.1293G=	NP_005154.2:p.Ser431=
XM_005267401.1:c.1293G=	XP_005267458.1:p.Ser431=
XM_011536543.1:c.1293G=	XP_011534845.1:p.Ser431=
XR_002957536.1:n.3010G=
NM_001014431.2:c.1293G=	NP_001014431.1:p.Ser431=
NM_001014432.2:c.1293G=	NP_001014432.1:p.Ser431=
NM_001382430.1:c.1293G= MANE Select	NP_001369359.1:p.Ser431=
NM_001382431.1:c.1293G=	NP_001369360.1:p.Ser431=
NM_001382432.1:c.1293G=	NP_001369361.1:p.Ser431=
NM_001382433.1:c.1293G=	NP_001369362.1:p.Ser431=