Canonical Allele Identifier: CA2335910008

Gene: AKT2

Linked Data

• dbSNP Id: rs1600131670
• gnomAD v3: 19-40285335-G-T
• gnomAD v4: 19-40285335-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285335G>T , CM000681.2:g.40285335G>T	GRCh38
NC_000019.9:g.40791242G>T , CM000681.1:g.40791242G>T	GRCh37
NC_000019.8:g.45483082G>T	NCBI36
NG_012038.2:g.5024C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-239C>A MANE Select	ENSP00000375892.2:n.-239C>A
ENST00000391844.8:c.-285C>A	ENSP00000375719.4:n.-285C>A
ENST00000392038.6:c.-239C>A	ENSP00000375892.2:n.-239C>A
ENST00000424901.5:c.-239C>A	ENSP00000399532.2:n.-239C>A
ENST00000578123.5:c.-85+113C>A	ENSP00000462022.1:n.-85+113C>A
ENST00000579047.5:c.-295C>A	ENSP00000471369.1:n.-295C>A
ENST00000584288.5:c.-378C>A	ENSP00000462469.1:n.-378C>A
NM_001243027.2:c.-388C>A	NP_001229956.1:n.-388C>A
NM_001243028.2:c.-295C>A	NP_001229957.1:n.-295C>A
NM_001626.5:c.-239C>A	NP_001617.1:n.-239C>A
XM_011526620.1:c.-85+113C>A	XP_011524922.1:n.-85+113C>A
XM_011526622.1:c.-239C>A	XP_011524924.1:n.-239C>A
XM_011526622.2:c.-239C>A	XP_011524924.1:n.-239C>A
XM_024451417.1:c.-239C>A	XP_024307185.1:n.-239C>A
NM_001626.6:c.-239C>A MANE Select	NP_001617.1:n.-239C>A
NM_001243027.3:c.-388C>A	NP_001229956.1:n.-388C>A
NM_001243028.3:c.-295C>A	NP_001229957.1:n.-295C>A