Canonical Allele Identifier: CA2335909943

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285279_40285297delinsACGGCGCCGGCAGCGGCAG , CM000681.2:g.40285279_40285297delinsACGGCGCCGGCAGCGGCAG	GRCh38
NC_000019.9:g.40791186_40791204delinsACGGCGCCGGCAGCGGCAG , CM000681.1:g.40791186_40791204delinsACGGCGCCGGCAGCGGCAG	GRCh37
NC_000019.8:g.45483026_45483044delinsACGGCGCCGGCAGCGGCAG	NCBI36
NG_012038.2:g.5062_5080delinsCTGCCGCTGCCGGCGCCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-201_-183delinsCTGCCGCTGCCGGCGCCGT MANE Select	ENSP00000375892.2:n.-201_-183delinsCTGCCGCTGCCGGCGCCGT
ENST00000391844.8:c.-247_-229delinsCTGCCGCTGCCGGCGCCGT	ENSP00000375719.4:n.-247_-229delinsCTGCCGCTGCCGGCGCCGT
ENST00000392038.6:c.-201_-183delinsCTGCCGCTGCCGGCGCCGT	ENSP00000375892.2:n.-201_-183delinsCTGCCGCTGCCGGCGCCGT
ENST00000424901.5:c.-201_-183delinsCTGCCGCTGCCGGCGCCGT	ENSP00000399532.2:n.-201_-183delinsCTGCCGCTGCCGGCGCCGT
ENST00000578123.5:c.-85+151_-85+169delinsCTGCCGCTGCCGGCGCCGT	ENSP00000462022.1:n.-85+151_-85+169delinsCTGCCGCTGCCGGCGCCGT
ENST00000579047.5:c.-257_-239delinsCTGCCGCTGCCGGCGCCGT	ENSP00000471369.1:n.-257_-239delinsCTGCCGCTGCCGGCGCCGT
ENST00000584288.5:c.-340_-322delinsCTGCCGCTGCCGGCGCCGT	ENSP00000462469.1:n.-340_-322delinsCTGCCGCTGCCGGCGCCGT
NM_001243027.2:c.-350_-332delinsCTGCCGCTGCCGGCGCCGT	NP_001229956.1:n.-350_-332delinsCTGCCGCTGCCGGCGCCGT
NM_001243028.2:c.-257_-239delinsCTGCCGCTGCCGGCGCCGT	NP_001229957.1:n.-257_-239delinsCTGCCGCTGCCGGCGCCGT
NM_001626.5:c.-201_-183delinsCTGCCGCTGCCGGCGCCGT	NP_001617.1:n.-201_-183delinsCTGCCGCTGCCGGCGCCGT
XM_011526620.1:c.-85+151_-85+169delinsCTGCCGCTGCCGGCGCCGT	XP_011524922.1:n.-85+151_-85+169delinsCTGCCGCTGCCGGCGCCGT
XM_011526622.1:c.-201_-183delinsCTGCCGCTGCCGGCGCCGT	XP_011524924.1:n.-201_-183delinsCTGCCGCTGCCGGCGCCGT
XM_011526622.2:c.-201_-183delinsCTGCCGCTGCCGGCGCCGT	XP_011524924.1:n.-201_-183delinsCTGCCGCTGCCGGCGCCGT
XM_024451417.1:c.-201_-183delinsCTGCCGCTGCCGGCGCCGT	XP_024307185.1:n.-201_-183delinsCTGCCGCTGCCGGCGCCGT
NM_001626.6:c.-201_-183delinsCTGCCGCTGCCGGCGCCGT MANE Select	NP_001617.1:n.-201_-183delinsCTGCCGCTGCCGGCGCCGT
NM_001243027.3:c.-350_-332delinsCTGCCGCTGCCGGCGCCGT	NP_001229956.1:n.-350_-332delinsCTGCCGCTGCCGGCGCCGT
NM_001243028.3:c.-257_-239delinsCTGCCGCTGCCGGCGCCGT	NP_001229957.1:n.-257_-239delinsCTGCCGCTGCCGGCGCCGT