Canonical Allele Identifier: CA2335909929

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285266_40285290delinsCCCGGCAGCGGCAACGGCGCCGGCA , CM000681.2:g.40285266_40285290delinsCCCGGCAGCGGCAACGGCGCCGGCA	GRCh38
NC_000019.9:g.40791173_40791197delinsCCCGGCAGCGGCAACGGCGCCGGCA , CM000681.1:g.40791173_40791197delinsCCCGGCAGCGGCAACGGCGCCGGCA	GRCh37
NC_000019.8:g.45483013_45483037delinsCCCGGCAGCGGCAACGGCGCCGGCA	NCBI36
NG_012038.2:g.5069_5093delinsTGCCGGCGCCGTTGCCGCTGCCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG MANE Select	ENSP00000375892.2:n.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG
ENST00000391844.8:c.-240_-216delinsTGCCGGCGCCGTTGCCGCTGCCGGG	ENSP00000375719.4:n.-240_-216delinsTGCCGGCGCCGTTGCCGCTGCCGGG
ENST00000392038.6:c.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG	ENSP00000375892.2:n.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG
ENST00000424901.5:c.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG	ENSP00000399532.2:n.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG
ENST00000578123.5:c.-85+158_-85+182delinsTGCCGGCGCCGTTGCCGCTGCCGGG	ENSP00000462022.1:n.-85+158_-85+182delinsTGCCGGCGCCGTTGCCGCTG...
ENST00000579047.5:c.-250_-226delinsTGCCGGCGCCGTTGCCGCTGCCGGG	ENSP00000471369.1:n.-250_-226delinsTGCCGGCGCCGTTGCCGCTGCCGGG
ENST00000584288.5:c.-333_-309delinsTGCCGGCGCCGTTGCCGCTGCCGGG	ENSP00000462469.1:n.-333_-309delinsTGCCGGCGCCGTTGCCGCTGCCGGG
NM_001243027.2:c.-343_-319delinsTGCCGGCGCCGTTGCCGCTGCCGGG	NP_001229956.1:n.-343_-319delinsTGCCGGCGCCGTTGCCGCTGCCGGG
NM_001243028.2:c.-250_-226delinsTGCCGGCGCCGTTGCCGCTGCCGGG	NP_001229957.1:n.-250_-226delinsTGCCGGCGCCGTTGCCGCTGCCGGG
NM_001626.5:c.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG	NP_001617.1:n.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG
XM_011526620.1:c.-85+158_-85+182delinsTGCCGGCGCCGTTGCCGCTGCCGGG	XP_011524922.1:n.-85+158_-85+182delinsTGCCGGCGCCGTTGCCGCTGCCG...
XM_011526622.1:c.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG	XP_011524924.1:n.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG
XM_011526622.2:c.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG	XP_011524924.1:n.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG
XM_024451417.1:c.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG	XP_024307185.1:n.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG
NM_001626.6:c.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG MANE Select	NP_001617.1:n.-194_-170delinsTGCCGGCGCCGTTGCCGCTGCCGGG
NM_001243027.3:c.-343_-319delinsTGCCGGCGCCGTTGCCGCTGCCGGG	NP_001229956.1:n.-343_-319delinsTGCCGGCGCCGTTGCCGCTGCCGGG
NM_001243028.3:c.-250_-226delinsTGCCGGCGCCGTTGCCGCTGCCGGG	NP_001229957.1:n.-250_-226delinsTGCCGGCGCCGTTGCCGCTGCCGGG