Canonical Allele Identifier: CA308376403

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40235996G>A , CM000681.2:g.40235996G>A	GRCh38
NC_000019.9:g.40741903G>A , CM000681.1:g.40741903G>A	GRCh37
NC_000019.8:g.45433743G>A	NCBI36
NG_012038.2:g.54363C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.1069C>T MANE Select	ENSP00000375892.2:p.Arg357Cys
ENST00000578615.6:c.948C>T
ENST00000311278.10:c.940C>T	ENSP00000309428.6:p.Arg314Cys
ENST00000391844.8:c.*683C>T	ENSP00000375719.4:n.*683C>T
ENST00000391845.6:n.534C>T
ENST00000392038.6:c.1069C>T	ENSP00000375892.2:p.Arg357Cys
ENST00000424901.5:c.940C>T	ENSP00000399532.2:p.Arg314Cys
ENST00000476247.6:c.76C>T	ENSP00000463368.1:p.Arg26Cys
ENST00000476266.5:n.1397C>T
ENST00000483166.5:n.2540C>T
ENST00000489375.5:c.36C>T
ENST00000496089.6:n.488C>T
ENST00000578615.5:c.637C>T	ENSP00000463262.1:p.Arg213Cys
ENST00000579047.5:c.883C>T	ENSP00000471369.1:p.Arg295Cys
ENST00000584288.5:c.*683C>T	ENSP00000462469.1:n.*683C>T
NM_001243027.2:c.883C>T	NP_001229956.1:p.Arg295Cys
NM_001243028.2:c.883C>T	NP_001229957.1:p.Arg295Cys
NM_001626.5:c.1069C>T	NP_001617.1:p.Arg357Cys
XM_011526614.1:c.1069C>T	XP_011524916.1:p.Arg357Cys
XM_011526615.1:c.1069C>T	XP_011524917.1:p.Arg357Cys
XM_011526616.1:c.1069C>T	XP_011524918.1:p.Arg357Cys
XM_011526617.1:c.1069C>T	XP_011524919.1:p.Arg357Cys
XM_011526618.1:c.1069C>T	XP_011524920.1:p.Arg357Cys
XM_011526619.1:c.1069C>T	XP_011524921.1:p.Arg357Cys
XM_011526620.1:c.1069C>T	XP_011524922.1:p.Arg357Cys
XM_011526621.1:c.1069C>T	XP_011524923.1:p.Arg357Cys
XM_011526622.1:c.1069C>T	XP_011524924.1:p.Arg357Cys
NM_001330511.1:c.940C>T	NP_001317440.1:p.Arg314Cys
XM_011526622.2:c.1069C>T	XP_011524924.1:p.Arg357Cys
XM_017026470.2:c.1069C>T	XP_016881959.1:p.Arg357Cys
XM_024451416.1:c.1069C>T	XP_024307184.1:p.Arg357Cys
XM_024451417.1:c.940C>T	XP_024307185.1:p.Arg314Cys
NM_001626.6:c.1069C>T MANE Select	NP_001617.1:p.Arg357Cys
NM_001243027.3:c.883C>T	NP_001229956.1:p.Arg295Cys
NM_001243028.3:c.883C>T	NP_001229957.1:p.Arg295Cys