Canonical Allele Identifier: CA2585108862

Gene: AKT2

Linked Data

• gnomAD v4: 19-40285267-C-CCGGCAGCGGCAACGGCGCCGGCAGCGGCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285272_40285301dup , CM000681.2:g.40285272_40285301dup	GRCh38
NC_000019.9:g.40791179_40791208dup , CM000681.1:g.40791179_40791208dup	GRCh37
NC_000019.8:g.45483019_45483048dup	NCBI36
NG_012038.2:g.5062_5091dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-201_-172dup MANE Select	ENSP00000375892.2:n.-201_-172dup
ENST00000391844.8:c.-247_-218dup	ENSP00000375719.4:n.-247_-218dup
ENST00000392038.6:c.-201_-172dup	ENSP00000375892.2:n.-201_-172dup
ENST00000424901.5:c.-201_-172dup	ENSP00000399532.2:n.-201_-172dup
ENST00000578123.5:c.-85+151_-85+180dup	ENSP00000462022.1:n.-85+151_-85+180dup
ENST00000579047.5:c.-257_-228dup	ENSP00000471369.1:n.-257_-228dup
ENST00000584288.5:c.-340_-311dup	ENSP00000462469.1:n.-340_-311dup
NM_001243027.2:c.-350_-321dup	NP_001229956.1:n.-350_-321dup
NM_001243028.2:c.-257_-228dup	NP_001229957.1:n.-257_-228dup
NM_001626.5:c.-201_-172dup	NP_001617.1:n.-201_-172dup
XM_011526620.1:c.-85+151_-85+180dup	XP_011524922.1:n.-85+151_-85+180dup
XM_011526622.1:c.-201_-172dup	XP_011524924.1:n.-201_-172dup
XM_011526622.2:c.-201_-172dup	XP_011524924.1:n.-201_-172dup
XM_024451417.1:c.-201_-172dup	XP_024307185.1:n.-201_-172dup
NM_001626.6:c.-201_-172dup MANE Select	NP_001617.1:n.-201_-172dup
NM_001243027.3:c.-350_-321dup	NP_001229956.1:n.-350_-321dup
NM_001243028.3:c.-257_-228dup	NP_001229957.1:n.-257_-228dup