Canonical Allele Identifier: CA2335909994

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285323G= , CM000681.2:g.40285323G=	GRCh38
NC_000019.9:g.40791230G= , CM000681.1:g.40791230G=	GRCh37
NC_000019.8:g.45483070G=	NCBI36
NG_012038.2:g.5036C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-227C= MANE Select	ENSP00000375892.2:n.-227C=
ENST00000391844.8:c.-273C=	ENSP00000375719.4:n.-273C=
ENST00000392038.6:c.-227C=	ENSP00000375892.2:n.-227C=
ENST00000424901.5:c.-227C=	ENSP00000399532.2:n.-227C=
ENST00000578123.5:c.-85+125C=	ENSP00000462022.1:n.-85+125C=
ENST00000579047.5:c.-283C=	ENSP00000471369.1:n.-283C=
ENST00000584288.5:c.-366C=	ENSP00000462469.1:n.-366C=
NM_001243027.2:c.-376C=	NP_001229956.1:n.-376C=
NM_001243028.2:c.-283C=	NP_001229957.1:n.-283C=
NM_001626.5:c.-227C=	NP_001617.1:n.-227C=
XM_011526620.1:c.-85+125C=	XP_011524922.1:n.-85+125C=
XM_011526622.1:c.-227C=	XP_011524924.1:n.-227C=
XM_011526622.2:c.-227C=	XP_011524924.1:n.-227C=
XM_024451417.1:c.-227C=	XP_024307185.1:n.-227C=
NM_001626.6:c.-227C= MANE Select	NP_001617.1:n.-227C=
NM_001243027.3:c.-376C=	NP_001229956.1:n.-376C=
NM_001243028.3:c.-283C=	NP_001229957.1:n.-283C=