Canonical Allele Identifier: CA2335887785

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40238115_40238116delinsAG , CM000681.2:g.40238115_40238116delinsAG	GRCh38
NC_000019.9:g.40744022_40744023delinsAG , CM000681.1:g.40744022_40744023delinsAG	GRCh37
NC_000019.8:g.45435862_45435863delinsAG	NCBI36
NG_012038.2:g.52243_52244delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.709-25_709-24delinsCT MANE Select	ENSP00000375892.2:n.709-25_709-24delinsCT
ENST00000578615.6:c.588-25_588-24delinsCT
ENST00000311278.10:c.709-25_709-24delinsCT	ENSP00000309428.6:n.709-25_709-24delinsCT
ENST00000391844.8:c.*323-25_*323-24delinsCT	ENSP00000375719.4:n.*323-25_*323-24delinsCT
ENST00000391845.6:n.174-25_174-24delinsCT
ENST00000392038.6:c.709-25_709-24delinsCT	ENSP00000375892.2:n.709-25_709-24delinsCT
ENST00000424901.5:c.709-25_709-24delinsCT	ENSP00000399532.2:n.709-25_709-24delinsCT
ENST00000476266.5:n.1037-25_1037-24delinsCT
ENST00000480878.6:n.136-25_136-24delinsCT
ENST00000483166.5:n.597-25_597-24delinsCT
ENST00000578282.5:n.102-25_102-24delinsCT
ENST00000578310.1:c.75-1731_75-1730delinsCT
ENST00000578615.5:c.277-25_277-24delinsCT	ENSP00000463262.1:n.277-25_277-24delinsCT
ENST00000579047.5:c.523-25_523-24delinsCT	ENSP00000471369.1:n.523-25_523-24delinsCT
ENST00000579345.5:n.229-25_229-24delinsCT
ENST00000580878.1:n.366-25_366-24delinsCT
ENST00000584288.5:c.*323-25_*323-24delinsCT	ENSP00000462469.1:n.*323-25_*323-24delinsCT
ENST00000601166.5:c.453-25_453-24delinsCT	ENSP00000472371.1:n.453-25_453-24delinsCT
NM_001243027.2:c.523-25_523-24delinsCT	NP_001229956.1:n.523-25_523-24delinsCT
NM_001243028.2:c.523-25_523-24delinsCT	NP_001229957.1:n.523-25_523-24delinsCT
NM_001626.5:c.709-25_709-24delinsCT	NP_001617.1:n.709-25_709-24delinsCT
XM_011526614.1:c.709-25_709-24delinsCT	XP_011524916.1:n.709-25_709-24delinsCT
XM_011526615.1:c.709-25_709-24delinsCT	XP_011524917.1:n.709-25_709-24delinsCT
XM_011526616.1:c.709-25_709-24delinsCT	XP_011524918.1:n.709-25_709-24delinsCT
XM_011526617.1:c.709-25_709-24delinsCT	XP_011524919.1:n.709-25_709-24delinsCT
XM_011526618.1:c.709-25_709-24delinsCT	XP_011524920.1:n.709-25_709-24delinsCT
XM_011526619.1:c.709-25_709-24delinsCT	XP_011524921.1:n.709-25_709-24delinsCT
XM_011526620.1:c.709-25_709-24delinsCT	XP_011524922.1:n.709-25_709-24delinsCT
XM_011526621.1:c.709-25_709-24delinsCT	XP_011524923.1:n.709-25_709-24delinsCT
XM_011526622.1:c.709-25_709-24delinsCT	XP_011524924.1:n.709-25_709-24delinsCT
NM_001330511.1:c.709-25_709-24delinsCT	NP_001317440.1:n.709-25_709-24delinsCT
XM_011526622.2:c.709-25_709-24delinsCT	XP_011524924.1:n.709-25_709-24delinsCT
XM_017026470.2:c.709-25_709-24delinsCT	XP_016881959.1:n.709-25_709-24delinsCT
XM_024451416.1:c.709-25_709-24delinsCT	XP_024307184.1:n.709-25_709-24delinsCT
XM_024451417.1:c.709-25_709-24delinsCT	XP_024307185.1:n.709-25_709-24delinsCT
NM_001626.6:c.709-25_709-24delinsCT MANE Select	NP_001617.1:n.709-25_709-24delinsCT
NM_001243027.3:c.523-25_523-24delinsCT	NP_001229956.1:n.523-25_523-24delinsCT
NM_001243028.3:c.523-25_523-24delinsCT	NP_001229957.1:n.523-25_523-24delinsCT