Canonical Allele Identifier: CA2335909977

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285304C= , CM000681.2:g.40285304C=	GRCh38
NC_000019.9:g.40791211C= , CM000681.1:g.40791211C=	GRCh37
NC_000019.8:g.45483051C=	NCBI36
NG_012038.2:g.5055G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-208G= MANE Select	ENSP00000375892.2:n.-208G=
ENST00000391844.8:c.-254G=	ENSP00000375719.4:n.-254G=
ENST00000392038.6:c.-208G=	ENSP00000375892.2:n.-208G=
ENST00000424901.5:c.-208G=	ENSP00000399532.2:n.-208G=
ENST00000578123.5:c.-85+144G=	ENSP00000462022.1:n.-85+144G=
ENST00000579047.5:c.-264G=	ENSP00000471369.1:n.-264G=
ENST00000584288.5:c.-347G=	ENSP00000462469.1:n.-347G=
NM_001243027.2:c.-357G=	NP_001229956.1:n.-357G=
NM_001243028.2:c.-264G=	NP_001229957.1:n.-264G=
NM_001626.5:c.-208G=	NP_001617.1:n.-208G=
XM_011526620.1:c.-85+144G=	XP_011524922.1:n.-85+144G=
XM_011526622.1:c.-208G=	XP_011524924.1:n.-208G=
XM_011526622.2:c.-208G=	XP_011524924.1:n.-208G=
XM_024451417.1:c.-208G=	XP_024307185.1:n.-208G=
NM_001626.6:c.-208G= MANE Select	NP_001617.1:n.-208G=
NM_001243027.3:c.-357G=	NP_001229956.1:n.-357G=
NM_001243028.3:c.-264G=	NP_001229957.1:n.-264G=