Canonical Allele Identifier: CA9441481

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40235119G>A , CM000681.2:g.40235119G>A	GRCh38
NC_000019.9:g.40741026G>A , CM000681.1:g.40741026G>A	GRCh37
NC_000019.8:g.45432866G>A	NCBI36
NG_012038.2:g.55240C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001626.6:c.1292C>T MANE Select	NP_001617.1:p.Thr431Met
ENST00000392038.7:c.1292C>T MANE Select	ENSP00000375892.2:p.Thr431Met
NM_001243027.2:c.1106C>T	NP_001229956.1:p.Thr369Met
NM_001243027.3:c.1106C>T	NP_001229956.1:p.Thr369Met
NM_001243028.2:c.1106C>T	NP_001229957.1:p.Thr369Met
NM_001243028.3:c.1106C>T	NP_001229957.1:p.Thr369Met
NM_001330511.1:c.1163C>T	NP_001317440.1:p.Thr388Met
NM_001626.5:c.1292C>T	NP_001617.1:p.Thr431Met
ENST00000311278.10:c.1163C>T	ENSP00000309428.6:p.Thr388Met
ENST00000391844.8:c.*906C>T	ENSP00000375719.4:n.*906C>T
ENST00000392038.6:c.1292C>T	ENSP00000375892.2:p.Thr431Met
ENST00000424901.5:c.1163C>T	ENSP00000399532.2:p.Thr388Met
ENST00000476247.6:c.299C>T	ENSP00000463368.1:p.Thr100Met
ENST00000476266.5:n.1620C>T
ENST00000483166.5:n.2763C>T
ENST00000489375.5:c.376C>T
ENST00000496089.6:n.711C>T
ENST00000497948.5:c.186C>T
ENST00000578615.5:c.860C>T	ENSP00000463262.1:p.Thr287Met
ENST00000578615.6:c.1171C>T
ENST00000579047.5:c.1106C>T	ENSP00000471369.1:p.Thr369Met
ENST00000584288.5:c.*906C>T	ENSP00000462469.1:n.*906C>T
XM_011526614.1:c.1292C>T	XP_011524916.1:p.Thr431Met
XM_011526615.1:c.1292C>T	XP_011524917.1:p.Thr431Met
XM_011526616.1:c.1292C>T	XP_011524918.1:p.Thr431Met
XM_011526617.1:c.1292C>T	XP_011524919.1:p.Thr431Met
XM_011526618.1:c.1292C>T	XP_011524920.1:p.Thr431Met
XM_011526619.1:c.1292C>T	XP_011524921.1:p.Thr431Met
XM_011526620.1:c.1292C>T	XP_011524922.1:p.Thr431Met
XM_011526621.1:c.1292C>T	XP_011524923.1:p.Thr431Met
XM_017026470.2:c.1292C>T	XP_016881959.1:p.Thr431Met
XM_024451416.1:c.1292C>T	XP_024307184.1:p.Thr431Met
XM_024451417.1:c.1163C>T	XP_024307185.1:p.Thr388Met