Canonical Allele Identifier: CA2335909993

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285322G= , CM000681.2:g.40285322G=	GRCh38
NC_000019.9:g.40791229G= , CM000681.1:g.40791229G=	GRCh37
NC_000019.8:g.45483069G=	NCBI36
NG_012038.2:g.5037C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-226C= MANE Select	ENSP00000375892.2:n.-226C=
ENST00000391844.8:c.-272C=	ENSP00000375719.4:n.-272C=
ENST00000392038.6:c.-226C=	ENSP00000375892.2:n.-226C=
ENST00000424901.5:c.-226C=	ENSP00000399532.2:n.-226C=
ENST00000578123.5:c.-85+126C=	ENSP00000462022.1:n.-85+126C=
ENST00000579047.5:c.-282C=	ENSP00000471369.1:n.-282C=
ENST00000584288.5:c.-365C=	ENSP00000462469.1:n.-365C=
NM_001243027.2:c.-375C=	NP_001229956.1:n.-375C=
NM_001243028.2:c.-282C=	NP_001229957.1:n.-282C=
NM_001626.5:c.-226C=	NP_001617.1:n.-226C=
XM_011526620.1:c.-85+126C=	XP_011524922.1:n.-85+126C=
XM_011526622.1:c.-226C=	XP_011524924.1:n.-226C=
XM_011526622.2:c.-226C=	XP_011524924.1:n.-226C=
XM_024451417.1:c.-226C=	XP_024307185.1:n.-226C=
NM_001626.6:c.-226C= MANE Select	NP_001617.1:n.-226C=
NM_001243027.3:c.-375C=	NP_001229956.1:n.-375C=
NM_001243028.3:c.-282C=	NP_001229957.1:n.-282C=