Canonical Allele Identifier: CA2335909949

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285285_40285300delinsCCGGCAGCGGCAGCGG , CM000681.2:g.40285285_40285300delinsCCGGCAGCGGCAGCGG	GRCh38
NC_000019.9:g.40791192_40791207delinsCCGGCAGCGGCAGCGG , CM000681.1:g.40791192_40791207delinsCCGGCAGCGGCAGCGG	GRCh37
NC_000019.8:g.45483032_45483047delinsCCGGCAGCGGCAGCGG	NCBI36
NG_012038.2:g.5059_5074delinsCCGCTGCCGCTGCCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-204_-189delinsCCGCTGCCGCTGCCGG MANE Select	ENSP00000375892.2:n.-204_-189delinsCCGCTGCCGCTGCCGG
ENST00000391844.8:c.-250_-235delinsCCGCTGCCGCTGCCGG	ENSP00000375719.4:n.-250_-235delinsCCGCTGCCGCTGCCGG
ENST00000392038.6:c.-204_-189delinsCCGCTGCCGCTGCCGG	ENSP00000375892.2:n.-204_-189delinsCCGCTGCCGCTGCCGG
ENST00000424901.5:c.-204_-189delinsCCGCTGCCGCTGCCGG	ENSP00000399532.2:n.-204_-189delinsCCGCTGCCGCTGCCGG
ENST00000578123.5:c.-85+148_-85+163delinsCCGCTGCCGCTGCCGG	ENSP00000462022.1:n.-85+148_-85+163delinsCCGCTGCCGCTGCCGG
ENST00000579047.5:c.-260_-245delinsCCGCTGCCGCTGCCGG	ENSP00000471369.1:n.-260_-245delinsCCGCTGCCGCTGCCGG
ENST00000584288.5:c.-343_-328delinsCCGCTGCCGCTGCCGG	ENSP00000462469.1:n.-343_-328delinsCCGCTGCCGCTGCCGG
NM_001243027.2:c.-353_-338delinsCCGCTGCCGCTGCCGG	NP_001229956.1:n.-353_-338delinsCCGCTGCCGCTGCCGG
NM_001243028.2:c.-260_-245delinsCCGCTGCCGCTGCCGG	NP_001229957.1:n.-260_-245delinsCCGCTGCCGCTGCCGG
NM_001626.5:c.-204_-189delinsCCGCTGCCGCTGCCGG	NP_001617.1:n.-204_-189delinsCCGCTGCCGCTGCCGG
XM_011526620.1:c.-85+148_-85+163delinsCCGCTGCCGCTGCCGG	XP_011524922.1:n.-85+148_-85+163delinsCCGCTGCCGCTGCCGG
XM_011526622.1:c.-204_-189delinsCCGCTGCCGCTGCCGG	XP_011524924.1:n.-204_-189delinsCCGCTGCCGCTGCCGG
XM_011526622.2:c.-204_-189delinsCCGCTGCCGCTGCCGG	XP_011524924.1:n.-204_-189delinsCCGCTGCCGCTGCCGG
XM_024451417.1:c.-204_-189delinsCCGCTGCCGCTGCCGG	XP_024307185.1:n.-204_-189delinsCCGCTGCCGCTGCCGG
NM_001626.6:c.-204_-189delinsCCGCTGCCGCTGCCGG MANE Select	NP_001617.1:n.-204_-189delinsCCGCTGCCGCTGCCGG
NM_001243027.3:c.-353_-338delinsCCGCTGCCGCTGCCGG	NP_001229956.1:n.-353_-338delinsCCGCTGCCGCTGCCGG
NM_001243028.3:c.-260_-245delinsCCGCTGCCGCTGCCGG	NP_001229957.1:n.-260_-245delinsCCGCTGCCGCTGCCGG