Canonical Allele Identifier: CA2160966188

Gene: AKT1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104780214C= , CM000676.2:g.104780214C=	GRCh38
NC_000014.8:g.105246551C= , CM000676.1:g.105246551C=	GRCh37
NC_000014.7:g.104317596C=	NCBI36
NG_012188.1:g.20531G= , LRG_721:g.20531G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001382430.1:c.49G= MANE Select	NP_001369359.1:p.Glu17=
ENST00000649815.2:c.49G= MANE Select	ENSP00000497822.1:p.Glu17=
NM_001014431.1:c.49G=	NP_001014431.1:p.Glu17=
NM_001014431.2:c.49G=	NP_001014431.1:p.Glu17=
NM_001014432.1:c.49G= , LRG_721t1:c.49G=	NP_001014432.1:p.Glu17=
NM_001014432.2:c.49G=	NP_001014432.1:p.Glu17=
NM_001382431.1:c.49G=	NP_001369360.1:p.Glu17=
NM_001382432.1:c.49G=	NP_001369361.1:p.Glu17=
NM_001382433.1:c.49G=	NP_001369362.1:p.Glu17=
NM_005163.2:c.49G= , LRG_721t2:c.49G=	NP_005154.2:p.Glu17=
ENST00000349310.7:c.49G=	ENSP00000270202.4:p.Glu17=
ENST00000402615.6:c.49G=	ENSP00000385326.2:p.Glu17=
ENST00000407796.6:c.49G=	ENSP00000384293.2:p.Glu17=
ENST00000407796.7:c.49G=	ENSP00000384293.2:p.Glu17=
ENST00000553797.2:c.49G=	ENSP00000507566.1:p.Glu17=
ENST00000554192.6:c.49G=	ENSP00000450681.3:p.Glu17=
ENST00000554581.5:c.49G=	ENSP00000451828.1:p.Glu17=
ENST00000554585.6:c.49G=	ENSP00000481526.2:p.Glu17=
ENST00000554826.2:n.187G=
ENST00000554848.5:c.49G=	ENSP00000451166.1:p.Glu17=
ENST00000555380.1:n.80G=
ENST00000555458.6:c.49G=	ENSP00000451470.3:p.Glu17=
ENST00000555528.5:c.49G=	ENSP00000450688.1:p.Glu17=
ENST00000555926.1:c.49G=	ENSP00000451824.1:p.Glu17=
ENST00000610370.2:n.187G=
ENST00000682269.1:n.566G=
ENST00000683722.1:c.49G=	ENSP00000507879.1:p.Glu17=
XM_005267401.1:c.49G=	XP_005267458.1:p.Glu17=
XM_011536543.1:c.49G=	XP_011534845.1:p.Glu17=
XM_011536544.1:c.49G=	XP_011534846.1:p.Glu17=
XR_002957536.1:n.249G=