Canonical Allele Identifier: CA405867101

Gene: AKT2

Linked Data

• dbSNP Id: rs1974139755
• MyVariant Identifiers: chr19:g.40743943T>C (hg19) ; chr19:g.40238036T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40238036T>C , CM000681.2:g.40238036T>C	GRCh38
NC_000019.9:g.40743943T>C , CM000681.1:g.40743943T>C	GRCh37
NC_000019.8:g.45435783T>C	NCBI36
NG_012038.2:g.52323A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.764A>G MANE Select	ENSP00000375892.2:p.Tyr255Cys
ENST00000578615.6:c.643A>G
ENST00000311278.10:c.764A>G	ENSP00000309428.6:p.Tyr255Cys
ENST00000391844.8:c.*378A>G	ENSP00000375719.4:n.*378A>G
ENST00000391845.6:n.229A>G
ENST00000392038.6:c.764A>G	ENSP00000375892.2:p.Tyr255Cys
ENST00000424901.5:c.764A>G	ENSP00000399532.2:p.Tyr255Cys
ENST00000476266.5:n.1092A>G
ENST00000480878.6:n.191A>G
ENST00000483166.5:n.652A>G
ENST00000496089.6:n.31A>G
ENST00000578282.5:n.157A>G
ENST00000578310.1:c.75-1651A>G
ENST00000578615.5:c.332A>G	ENSP00000463262.1:p.Tyr111Cys
ENST00000579047.5:c.578A>G	ENSP00000471369.1:p.Tyr193Cys
ENST00000579345.5:n.284A>G
ENST00000580878.1:n.421A>G
ENST00000584288.5:c.*378A>G	ENSP00000462469.1:n.*378A>G
ENST00000601166.5:c.508A>G	ENSP00000472371.1:n.508A>G
NM_001243027.2:c.578A>G	NP_001229956.1:p.Tyr193Cys
NM_001243028.2:c.578A>G	NP_001229957.1:p.Tyr193Cys
NM_001626.5:c.764A>G	NP_001617.1:p.Tyr255Cys
XM_011526614.1:c.764A>G	XP_011524916.1:p.Tyr255Cys
XM_011526615.1:c.764A>G	XP_011524917.1:p.Tyr255Cys
XM_011526616.1:c.764A>G	XP_011524918.1:p.Tyr255Cys
XM_011526617.1:c.764A>G	XP_011524919.1:p.Tyr255Cys
XM_011526618.1:c.764A>G	XP_011524920.1:p.Tyr255Cys
XM_011526619.1:c.764A>G	XP_011524921.1:p.Tyr255Cys
XM_011526620.1:c.764A>G	XP_011524922.1:p.Tyr255Cys
XM_011526621.1:c.764A>G	XP_011524923.1:p.Tyr255Cys
XM_011526622.1:c.764A>G	XP_011524924.1:p.Tyr255Cys
NM_001330511.1:c.764A>G	NP_001317440.1:p.Tyr255Cys
XM_011526622.2:c.764A>G	XP_011524924.1:p.Tyr255Cys
XM_017026470.2:c.764A>G	XP_016881959.1:p.Tyr255Cys
XM_024451416.1:c.764A>G	XP_024307184.1:p.Tyr255Cys
XM_024451417.1:c.764A>G	XP_024307185.1:p.Tyr255Cys
NM_001626.6:c.764A>G MANE Select	NP_001617.1:p.Tyr255Cys
NM_001243027.3:c.578A>G	NP_001229956.1:p.Tyr193Cys
NM_001243028.3:c.578A>G	NP_001229957.1:p.Tyr193Cys