Canonical Allele Identifier: CA405867036

Gene: AKT2

Linked Data

• MyVariant Identifiers: chr19:g.40743922G>T (hg19) ; chr19:g.40238015G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40238015G>T , CM000681.2:g.40238015G>T	GRCh38
NC_000019.9:g.40743922G>T , CM000681.1:g.40743922G>T	GRCh37
NC_000019.8:g.45435762G>T	NCBI36
NG_012038.2:g.52344C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.785C>A MANE Select	ENSP00000375892.2:p.Ala262Asp
ENST00000578615.6:c.664C>A
ENST00000311278.10:c.785C>A	ENSP00000309428.6:p.Ala262Asp
ENST00000391844.8:c.*399C>A	ENSP00000375719.4:n.*399C>A
ENST00000391845.6:n.250C>A
ENST00000392038.6:c.785C>A	ENSP00000375892.2:p.Ala262Asp
ENST00000424901.5:c.785C>A	ENSP00000399532.2:p.Ala262Asp
ENST00000476266.5:n.1113C>A
ENST00000480878.6:n.212C>A
ENST00000483166.5:n.673C>A
ENST00000496089.6:n.52C>A
ENST00000578282.5:n.178C>A
ENST00000578310.1:c.75-1630C>A
ENST00000578615.5:c.353C>A	ENSP00000463262.1:p.Ala118Asp
ENST00000579047.5:c.599C>A	ENSP00000471369.1:p.Ala200Asp
ENST00000579345.5:n.305C>A
ENST00000580878.1:n.442C>A
ENST00000584288.5:c.*399C>A	ENSP00000462469.1:n.*399C>A
ENST00000601166.5:c.529C>A	ENSP00000472371.1:n.529C>A
NM_001243027.2:c.599C>A	NP_001229956.1:p.Ala200Asp
NM_001243028.2:c.599C>A	NP_001229957.1:p.Ala200Asp
NM_001626.5:c.785C>A	NP_001617.1:p.Ala262Asp
XM_011526614.1:c.785C>A	XP_011524916.1:p.Ala262Asp
XM_011526615.1:c.785C>A	XP_011524917.1:p.Ala262Asp
XM_011526616.1:c.785C>A	XP_011524918.1:p.Ala262Asp
XM_011526617.1:c.785C>A	XP_011524919.1:p.Ala262Asp
XM_011526618.1:c.785C>A	XP_011524920.1:p.Ala262Asp
XM_011526619.1:c.785C>A	XP_011524921.1:p.Ala262Asp
XM_011526620.1:c.785C>A	XP_011524922.1:p.Ala262Asp
XM_011526621.1:c.785C>A	XP_011524923.1:p.Ala262Asp
XM_011526622.1:c.785C>A	XP_011524924.1:p.Ala262Asp
NM_001330511.1:c.785C>A	NP_001317440.1:p.Ala262Asp
XM_011526622.2:c.785C>A	XP_011524924.1:p.Ala262Asp
XM_017026470.2:c.785C>A	XP_016881959.1:p.Ala262Asp
XM_024451416.1:c.785C>A	XP_024307184.1:p.Ala262Asp
XM_024451417.1:c.785C>A	XP_024307185.1:p.Ala262Asp
NM_001626.6:c.785C>A MANE Select	NP_001617.1:p.Ala262Asp
NM_001243027.3:c.599C>A	NP_001229956.1:p.Ala200Asp
NM_001243028.3:c.599C>A	NP_001229957.1:p.Ala200Asp