Canonical Allele Identifier: CA9441359

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40233606A>G , CM000681.2:g.40233606A>G	GRCh38
NC_000019.9:g.40739513A>G , CM000681.1:g.40739513A>G	GRCh37
NC_000019.8:g.45431353A>G	NCBI36
NG_012038.2:g.56753T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001626.6:c.*266T>C MANE Select	NP_001617.1:n.*266T>C
ENST00000392038.7:c.*266T>C MANE Select	ENSP00000375892.2:n.*266T>C
NM_001243027.2:c.*266T>C	NP_001229956.1:n.*266T>C
NM_001243027.3:c.*266T>C	NP_001229956.1:n.*266T>C
NM_001243028.2:c.*266T>C	NP_001229957.1:n.*266T>C
NM_001243028.3:c.*266T>C	NP_001229957.1:n.*266T>C
NM_001330511.1:c.*266T>C	NP_001317440.1:n.*266T>C
NM_001626.5:c.*266T>C	NP_001617.1:n.*266T>C
ENST00000392038.6:c.*266T>C	ENSP00000375892.2:n.*266T>C
ENST00000424901.5:c.*266T>C	ENSP00000399532.2:n.*266T>C
ENST00000476266.5:n.2040T>C
ENST00000483166.5:n.3183T>C
XM_011526614.1:c.*266T>C	XP_011524916.1:n.*266T>C
XM_011526615.1:c.*266T>C	XP_011524917.1:n.*266T>C
XM_011526616.1:c.*266T>C	XP_011524918.1:n.*266T>C
XM_011526617.1:c.*266T>C	XP_011524919.1:n.*266T>C
XM_011526618.1:c.*266T>C	XP_011524920.1:n.*266T>C
XM_011526619.1:c.*266T>C	XP_011524921.1:n.*266T>C
XM_011526620.1:c.*266T>C	XP_011524922.1:n.*266T>C
XM_011526621.1:c.*266T>C	XP_011524923.1:n.*266T>C
XM_017026470.2:c.*266T>C	XP_016881959.1:n.*266T>C
XM_024451416.1:c.*266T>C	XP_024307184.1:n.*266T>C
XM_024451417.1:c.*266T>C	XP_024307185.1:n.*266T>C