Canonical Allele Identifier: CA405865786

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40235125T>C , CM000681.2:g.40235125T>C	GRCh38
NC_000019.9:g.40741032T>C , CM000681.1:g.40741032T>C	GRCh37
NC_000019.8:g.45432872T>C	NCBI36
NG_012038.2:g.55234A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.1286A>G MANE Select	ENSP00000375892.2:p.Gln429Arg
ENST00000578615.6:c.1165A>G
ENST00000311278.10:c.1157A>G	ENSP00000309428.6:p.Gln386Arg
ENST00000391844.8:c.*900A>G	ENSP00000375719.4:n.*900A>G
ENST00000392038.6:c.1286A>G	ENSP00000375892.2:p.Gln429Arg
ENST00000424901.5:c.1157A>G	ENSP00000399532.2:p.Gln386Arg
ENST00000476247.6:c.293A>G	ENSP00000463368.1:p.Gln98Arg
ENST00000476266.5:n.1614A>G
ENST00000483166.5:n.2757A>G
ENST00000489375.5:c.370A>G
ENST00000496089.6:n.705A>G
ENST00000497948.5:c.180A>G
ENST00000578615.5:c.854A>G	ENSP00000463262.1:p.Gln285Arg
ENST00000579047.5:c.1100A>G	ENSP00000471369.1:p.Gln367Arg
ENST00000584288.5:c.*900A>G	ENSP00000462469.1:n.*900A>G
NM_001243027.2:c.1100A>G	NP_001229956.1:p.Gln367Arg
NM_001243028.2:c.1100A>G	NP_001229957.1:p.Gln367Arg
NM_001626.5:c.1286A>G	NP_001617.1:p.Gln429Arg
XM_011526614.1:c.1286A>G	XP_011524916.1:p.Gln429Arg
XM_011526615.1:c.1286A>G	XP_011524917.1:p.Gln429Arg
XM_011526616.1:c.1286A>G	XP_011524918.1:p.Gln429Arg
XM_011526617.1:c.1286A>G	XP_011524919.1:p.Gln429Arg
XM_011526618.1:c.1286A>G	XP_011524920.1:p.Gln429Arg
XM_011526619.1:c.1286A>G	XP_011524921.1:p.Gln429Arg
XM_011526620.1:c.1286A>G	XP_011524922.1:p.Gln429Arg
XM_011526621.1:c.1286A>G	XP_011524923.1:p.Gln429Arg
NM_001330511.1:c.1157A>G	NP_001317440.1:p.Gln386Arg
XM_017026470.2:c.1286A>G	XP_016881959.1:p.Gln429Arg
XM_024451416.1:c.1286A>G	XP_024307184.1:p.Gln429Arg
XM_024451417.1:c.1157A>G	XP_024307185.1:p.Gln386Arg
NM_001626.6:c.1286A>G MANE Select	NP_001617.1:p.Gln429Arg
NM_001243027.3:c.1100A>G	NP_001229956.1:p.Gln367Arg
NM_001243028.3:c.1100A>G	NP_001229957.1:p.Gln367Arg