Canonical Allele Identifier: CA405867026

Gene: AKT2

Linked Data

• MyVariant Identifiers: chr19:g.40743917C>A (hg19) ; chr19:g.40238010C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40238010C>A , CM000681.2:g.40238010C>A	GRCh38
NC_000019.9:g.40743917C>A , CM000681.1:g.40743917C>A	GRCh37
NC_000019.8:g.45435757C>A	NCBI36
NG_012038.2:g.52349G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.790G>T MANE Select	ENSP00000375892.2:p.Glu264Ter
ENST00000578615.6:c.669G>T
ENST00000311278.10:c.790G>T	ENSP00000309428.6:p.Glu264Ter
ENST00000391844.8:c.*404G>T	ENSP00000375719.4:n.*404G>T
ENST00000391845.6:n.255G>T
ENST00000392038.6:c.790G>T	ENSP00000375892.2:p.Glu264Ter
ENST00000424901.5:c.790G>T	ENSP00000399532.2:p.Glu264Ter
ENST00000476266.5:n.1118G>T
ENST00000480878.6:n.217G>T
ENST00000483166.5:n.678G>T
ENST00000496089.6:n.57G>T
ENST00000578282.5:n.183G>T
ENST00000578310.1:c.75-1625G>T
ENST00000578615.5:c.358G>T	ENSP00000463262.1:p.Glu120Ter
ENST00000579047.5:c.604G>T	ENSP00000471369.1:p.Glu202Ter
ENST00000579345.5:n.310G>T
ENST00000580878.1:n.447G>T
ENST00000584288.5:c.*404G>T	ENSP00000462469.1:n.*404G>T
ENST00000601166.5:c.534G>T	ENSP00000472371.1:n.534G>T
NM_001243027.2:c.604G>T	NP_001229956.1:p.Glu202Ter
NM_001243028.2:c.604G>T	NP_001229957.1:p.Glu202Ter
NM_001626.5:c.790G>T	NP_001617.1:p.Glu264Ter
XM_011526614.1:c.790G>T	XP_011524916.1:p.Glu264Ter
XM_011526615.1:c.790G>T	XP_011524917.1:p.Glu264Ter
XM_011526616.1:c.790G>T	XP_011524918.1:p.Glu264Ter
XM_011526617.1:c.790G>T	XP_011524919.1:p.Glu264Ter
XM_011526618.1:c.790G>T	XP_011524920.1:p.Glu264Ter
XM_011526619.1:c.790G>T	XP_011524921.1:p.Glu264Ter
XM_011526620.1:c.790G>T	XP_011524922.1:p.Glu264Ter
XM_011526621.1:c.790G>T	XP_011524923.1:p.Glu264Ter
XM_011526622.1:c.790G>T	XP_011524924.1:p.Glu264Ter
NM_001330511.1:c.790G>T	NP_001317440.1:p.Glu264Ter
XM_011526622.2:c.790G>T	XP_011524924.1:p.Glu264Ter
XM_017026470.2:c.790G>T	XP_016881959.1:p.Glu264Ter
XM_024451416.1:c.790G>T	XP_024307184.1:p.Glu264Ter
XM_024451417.1:c.790G>T	XP_024307185.1:p.Glu264Ter
NM_001626.6:c.790G>T MANE Select	NP_001617.1:p.Glu264Ter
NM_001243027.3:c.604G>T	NP_001229956.1:p.Glu202Ter
NM_001243028.3:c.604G>T	NP_001229957.1:p.Glu202Ter