Canonical Allele Identifier: CA914326652

Gene: AKT2

Linked Data

• gnomAD v2: 19-40791231-CAG-C
• gnomAD v3: 19-40285324-CAG-C
• gnomAD v4: 19-40285324-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285325_40285326del , CM000681.2:g.40285325_40285326del	GRCh38
NC_000019.9:g.40791232_40791233del , CM000681.1:g.40791232_40791233del	GRCh37
NC_000019.8:g.45483072_45483073del	NCBI36
NG_012038.2:g.5033_5034del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-230_-229del MANE Select	ENSP00000375892.2:n.-230_-229del
ENST00000391844.8:c.-276_-275del	ENSP00000375719.4:n.-276_-275del
ENST00000392038.6:c.-230_-229del	ENSP00000375892.2:n.-230_-229del
ENST00000424901.5:c.-230_-229del	ENSP00000399532.2:n.-230_-229del
ENST00000578123.5:c.-85+122_-85+123del	ENSP00000462022.1:n.-85+122_-85+123del
ENST00000579047.5:c.-286_-285del	ENSP00000471369.1:n.-286_-285del
ENST00000584288.5:c.-369_-368del	ENSP00000462469.1:n.-369_-368del
NM_001243027.2:c.-379_-378del	NP_001229956.1:n.-379_-378del
NM_001243028.2:c.-286_-285del	NP_001229957.1:n.-286_-285del
NM_001626.5:c.-230_-229del	NP_001617.1:n.-230_-229del
XM_011526620.1:c.-85+122_-85+123del	XP_011524922.1:n.-85+122_-85+123del
XM_011526622.1:c.-230_-229del	XP_011524924.1:n.-230_-229del
XM_011526622.2:c.-230_-229del	XP_011524924.1:n.-230_-229del
XM_024451417.1:c.-230_-229del	XP_024307185.1:n.-230_-229del
NM_001626.6:c.-230_-229del MANE Select	NP_001617.1:n.-230_-229del
NM_001243027.3:c.-379_-378del	NP_001229956.1:n.-379_-378del
NM_001243028.3:c.-286_-285del	NP_001229957.1:n.-286_-285del