Canonical Allele Identifier: CA2335909950

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285285_40285309delinsCCGGCAGCGGCAGCGGCGGCGGCGA , CM000681.2:g.40285285_40285309delinsCCGGCAGCGGCAGCGGCGGCGGCGA	GRCh38
NC_000019.9:g.40791192_40791216delinsCCGGCAGCGGCAGCGGCGGCGGCGA , CM000681.1:g.40791192_40791216delinsCCGGCAGCGGCAGCGGCGGCGGCGA	GRCh37
NC_000019.8:g.45483032_45483056delinsCCGGCAGCGGCAGCGGCGGCGGCGA	NCBI36
NG_012038.2:g.5050_5074delinsTCGCCGCCGCCGCTGCCGCTGCCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG MANE Select	ENSP00000375892.2:n.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG
ENST00000391844.8:c.-259_-235delinsTCGCCGCCGCCGCTGCCGCTGCCGG	ENSP00000375719.4:n.-259_-235delinsTCGCCGCCGCCGCTGCCGCTGCCGG
ENST00000392038.6:c.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG	ENSP00000375892.2:n.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG
ENST00000424901.5:c.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG	ENSP00000399532.2:n.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG
ENST00000578123.5:c.-85+139_-85+163delinsTCGCCGCCGCCGCTGCCGCTGCCGG	ENSP00000462022.1:n.-85+139_-85+163delinsTCGCCGCCGCCGCTGCCGCT...
ENST00000579047.5:c.-269_-245delinsTCGCCGCCGCCGCTGCCGCTGCCGG	ENSP00000471369.1:n.-269_-245delinsTCGCCGCCGCCGCTGCCGCTGCCGG
ENST00000584288.5:c.-352_-328delinsTCGCCGCCGCCGCTGCCGCTGCCGG	ENSP00000462469.1:n.-352_-328delinsTCGCCGCCGCCGCTGCCGCTGCCGG
NM_001243027.2:c.-362_-338delinsTCGCCGCCGCCGCTGCCGCTGCCGG	NP_001229956.1:n.-362_-338delinsTCGCCGCCGCCGCTGCCGCTGCCGG
NM_001243028.2:c.-269_-245delinsTCGCCGCCGCCGCTGCCGCTGCCGG	NP_001229957.1:n.-269_-245delinsTCGCCGCCGCCGCTGCCGCTGCCGG
NM_001626.5:c.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG	NP_001617.1:n.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG
XM_011526620.1:c.-85+139_-85+163delinsTCGCCGCCGCCGCTGCCGCTGCCGG	XP_011524922.1:n.-85+139_-85+163delinsTCGCCGCCGCCGCTGCCGCTGCC...
XM_011526622.1:c.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG	XP_011524924.1:n.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG
XM_011526622.2:c.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG	XP_011524924.1:n.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG
XM_024451417.1:c.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG	XP_024307185.1:n.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG
NM_001626.6:c.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG MANE Select	NP_001617.1:n.-213_-189delinsTCGCCGCCGCCGCTGCCGCTGCCGG
NM_001243027.3:c.-362_-338delinsTCGCCGCCGCCGCTGCCGCTGCCGG	NP_001229956.1:n.-362_-338delinsTCGCCGCCGCCGCTGCCGCTGCCGG
NM_001243028.3:c.-269_-245delinsTCGCCGCCGCCGCTGCCGCTGCCGG	NP_001229957.1:n.-269_-245delinsTCGCCGCCGCCGCTGCCGCTGCCGG