Canonical Allele Identifier: CA2585108893

Gene: AKT2

Linked Data

• gnomAD v4: 19-40285289-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285289C>A , CM000681.2:g.40285289C>A	GRCh38
NC_000019.9:g.40791196C>A , CM000681.1:g.40791196C>A	GRCh37
NC_000019.8:g.45483036C>A	NCBI36
NG_012038.2:g.5070G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-193G>T MANE Select	ENSP00000375892.2:n.-193G>T
ENST00000391844.8:c.-239G>T	ENSP00000375719.4:n.-239G>T
ENST00000392038.6:c.-193G>T	ENSP00000375892.2:n.-193G>T
ENST00000424901.5:c.-193G>T	ENSP00000399532.2:n.-193G>T
ENST00000578123.5:c.-85+159G>T	ENSP00000462022.1:n.-85+159G>T
ENST00000579047.5:c.-249G>T	ENSP00000471369.1:n.-249G>T
ENST00000584288.5:c.-332G>T	ENSP00000462469.1:n.-332G>T
NM_001243027.2:c.-342G>T	NP_001229956.1:n.-342G>T
NM_001243028.2:c.-249G>T	NP_001229957.1:n.-249G>T
NM_001626.5:c.-193G>T	NP_001617.1:n.-193G>T
XM_011526620.1:c.-85+159G>T	XP_011524922.1:n.-85+159G>T
XM_011526622.1:c.-193G>T	XP_011524924.1:n.-193G>T
XM_011526622.2:c.-193G>T	XP_011524924.1:n.-193G>T
XM_024451417.1:c.-193G>T	XP_024307185.1:n.-193G>T
NM_001626.6:c.-193G>T MANE Select	NP_001617.1:n.-193G>T
NM_001243027.3:c.-342G>T	NP_001229956.1:n.-342G>T
NM_001243028.3:c.-249G>T	NP_001229957.1:n.-249G>T