Canonical Allele Identifier: CA2335896288

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40257052C= , CM000681.2:g.40257052C=	GRCh38
NC_000019.9:g.40762959C= , CM000681.1:g.40762959C=	GRCh37
NC_000019.8:g.45454799C=	NCBI36
NG_012038.2:g.33307G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001626.6:c.49G= MANE Select	NP_001617.1:p.Glu17=
ENST00000392038.7:c.49G= MANE Select	ENSP00000375892.2:p.Glu17=
NM_001243027.2:c.-138G=	NP_001229956.1:n.-138G=
NM_001243027.3:c.-138G=	NP_001229956.1:n.-138G=
NM_001243028.2:c.-138G=	NP_001229957.1:n.-138G=
NM_001243028.3:c.-138G=	NP_001229957.1:n.-138G=
NM_001330511.1:c.49G=	NP_001317440.1:p.Glu17=
NM_001626.5:c.49G=	NP_001617.1:p.Glu17=
ENST00000311278.10:c.49G=	ENSP00000309428.6:p.Glu17=
ENST00000358335.9:c.49G=	ENSP00000351095.5:p.Glu17=
ENST00000391844.8:c.-128G=	ENSP00000375719.4:n.-128G=
ENST00000392037.5:c.49G=	ENSP00000375891.1:p.Glu17=
ENST00000392038.6:c.49G=	ENSP00000375892.2:p.Glu17=
ENST00000416362.5:c.49G=	ENSP00000407999.1:p.Glu17=
ENST00000416994.6:c.49G=	ENSP00000392458.2:p.Glu17=
ENST00000423127.5:c.49G=	ENSP00000403842.1:p.Glu17=
ENST00000424901.5:c.49G=	ENSP00000399532.2:p.Glu17=
ENST00000427375.1:c.49G=	ENSP00000403890.1:p.Glu17=
ENST00000441941.6:c.49G=	ENSP00000396968.2:p.Glu17=
ENST00000452077.5:c.49G=	ENSP00000404083.1:p.Glu17=
ENST00000456441.5:c.49G=	ENSP00000396532.1:p.Glu17=
ENST00000486368.6:c.49G=	ENSP00000463686.1:p.Glu17=
ENST00000487537.3:n.154G=
ENST00000492463.6:c.-128G=	ENSP00000462776.1:n.-128G=
ENST00000537834.5:n.357G=
ENST00000578123.5:c.49G=	ENSP00000462022.1:p.Glu17=
ENST00000579047.5:c.-138G=	ENSP00000471369.1:n.-138G=
ENST00000580747.5:c.49G=	ENSP00000463806.2:p.Glu17=
ENST00000583859.5:c.49G=	ENSP00000462715.1:p.Glu17=
ENST00000584288.5:c.-128G=	ENSP00000462469.1:n.-128G=
ENST00000596634.5:c.49G=	ENSP00000470604.1:p.Glu17=
ENST00000672879.1:n.191G=
ENST00000672890.1:c.49G=	ENSP00000500412.1:p.Glu17=
XM_011526614.1:c.49G=	XP_011524916.1:p.Glu17=
XM_011526615.1:c.49G=	XP_011524917.1:p.Glu17=
XM_011526616.1:c.49G=	XP_011524918.1:p.Glu17=
XM_011526617.1:c.49G=	XP_011524919.1:p.Glu17=
XM_011526618.1:c.49G=	XP_011524920.1:p.Glu17=
XM_011526619.1:c.49G=	XP_011524921.1:p.Glu17=
XM_011526620.1:c.49G=	XP_011524922.1:p.Glu17=
XM_011526621.1:c.49G=	XP_011524923.1:p.Glu17=
XM_011526622.1:c.49G=	XP_011524924.1:p.Glu17=
XM_011526622.2:c.49G=	XP_011524924.1:p.Glu17=
XM_017026470.2:c.49G=	XP_016881959.1:p.Glu17=
XM_024451416.1:c.49G=	XP_024307184.1:p.Glu17=
XM_024451417.1:c.49G=	XP_024307185.1:p.Glu17=