Canonical Allele Identifier: CA2335909897

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285207C= , CM000681.2:g.40285207C=	GRCh38
NC_000019.9:g.40791114C= , CM000681.1:g.40791114C=	GRCh37
NC_000019.8:g.45482954C=	NCBI36
NG_012038.2:g.5152G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-111G= MANE Select	ENSP00000375892.2:n.-111G=
ENST00000358335.9:c.-111G=	ENSP00000351095.5:n.-111G=
ENST00000391844.8:c.-157G=	ENSP00000375719.4:n.-157G=
ENST00000392038.6:c.-111G=	ENSP00000375892.2:n.-111G=
ENST00000424901.5:c.-111G=	ENSP00000399532.2:n.-111G=
ENST00000578123.5:c.-85+241G=	ENSP00000462022.1:n.-85+241G=
ENST00000579047.5:c.-167G=	ENSP00000471369.1:n.-167G=
ENST00000584288.5:c.-250G=	ENSP00000462469.1:n.-250G=
NM_001243027.2:c.-260G=	NP_001229956.1:n.-260G=
NM_001243028.2:c.-167G=	NP_001229957.1:n.-167G=
NM_001626.5:c.-111G=	NP_001617.1:n.-111G=
XM_011526620.1:c.-85+241G=	XP_011524922.1:n.-85+241G=
XM_011526622.1:c.-111G=	XP_011524924.1:n.-111G=
XM_011526622.2:c.-111G=	XP_011524924.1:n.-111G=
XM_024451417.1:c.-111G=	XP_024307185.1:n.-111G=
NM_001626.6:c.-111G= MANE Select	NP_001617.1:n.-111G=
NM_001243027.3:c.-260G=	NP_001229956.1:n.-260G=
NM_001243028.3:c.-167G=	NP_001229957.1:n.-167G=