Canonical Allele Identifier: CA9441896

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40242579C>T , CM000681.2:g.40242579C>T	GRCh38
NC_000019.9:g.40748486C>T , CM000681.1:g.40748486C>T	GRCh37
NC_000019.8:g.45440326C>T	NCBI36
NG_012038.2:g.47780G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.396G>A MANE Select	ENSP00000375892.2:p.Thr132=
ENST00000487537.3:n.501G>A
ENST00000578615.6:c.341G>A
ENST00000672879.1:n.538G>A
ENST00000311278.10:c.396G>A	ENSP00000309428.6:p.Thr132=
ENST00000391844.8:c.*10G>A	ENSP00000375719.4:n.*10G>A
ENST00000392037.5:c.396G>A	ENSP00000375891.1:p.Thr132=
ENST00000392038.6:c.396G>A	ENSP00000375892.2:p.Thr132=
ENST00000416362.5:c.396G>A	ENSP00000407999.1:p.Thr132=
ENST00000424901.5:c.396G>A	ENSP00000399532.2:p.Thr132=
ENST00000441941.6:c.396G>A	ENSP00000396968.2:p.Thr132=
ENST00000452077.5:c.396G>A	ENSP00000404083.1:p.Thr132=
ENST00000476266.5:n.724G>A
ENST00000486368.6:c.396G>A	ENSP00000463686.1:p.Thr132=
ENST00000487537.2:n.221G>A
ENST00000491778.6:c.355G>A
ENST00000492463.6:c.*10G>A	ENSP00000462776.1:n.*10G>A
ENST00000537834.5:n.704G>A
ENST00000578615.5:c.30G>A	ENSP00000463262.1:p.Thr10=
ENST00000578975.1:n.1549G>A
ENST00000579047.5:c.210G>A	ENSP00000471369.1:p.Thr70=
ENST00000584288.5:c.*10G>A	ENSP00000462469.1:n.*10G>A
ENST00000596634.5:c.396G>A	ENSP00000470604.1:p.Thr132=
ENST00000601166.5:c.129G>A	ENSP00000472371.1:p.Thr43=
NM_001243027.2:c.210G>A	NP_001229956.1:p.Thr70=
NM_001243028.2:c.210G>A	NP_001229957.1:p.Thr70=
NM_001626.5:c.396G>A	NP_001617.1:p.Thr132=
XM_011526614.1:c.396G>A	XP_011524916.1:p.Thr132=
XM_011526615.1:c.396G>A	XP_011524917.1:p.Thr132=
XM_011526616.1:c.396G>A	XP_011524918.1:p.Thr132=
XM_011526617.1:c.396G>A	XP_011524919.1:p.Thr132=
XM_011526618.1:c.396G>A	XP_011524920.1:p.Thr132=
XM_011526619.1:c.396G>A	XP_011524921.1:p.Thr132=
XM_011526620.1:c.396G>A	XP_011524922.1:p.Thr132=
XM_011526621.1:c.396G>A	XP_011524923.1:p.Thr132=
XM_011526622.1:c.396G>A	XP_011524924.1:p.Thr132=
NM_001330511.1:c.396G>A	NP_001317440.1:p.Thr132=
XM_011526622.2:c.396G>A	XP_011524924.1:p.Thr132=
XM_017026470.2:c.396G>A	XP_016881959.1:p.Thr132=
XM_024451416.1:c.396G>A	XP_024307184.1:p.Thr132=
XM_024451417.1:c.396G>A	XP_024307185.1:p.Thr132=
NM_001626.6:c.396G>A MANE Select	NP_001617.1:p.Thr132=
NM_001243027.3:c.210G>A	NP_001229956.1:p.Thr70=
NM_001243028.3:c.210G>A	NP_001229957.1:p.Thr70=