Canonical Allele Identifier: CA2585108900

Gene: AKT2

Linked Data

• gnomAD v4: 19-40285295-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285295C>T , CM000681.2:g.40285295C>T	GRCh38
NC_000019.9:g.40791202C>T , CM000681.1:g.40791202C>T	GRCh37
NC_000019.8:g.45483042C>T	NCBI36
NG_012038.2:g.5064G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-199G>A MANE Select	ENSP00000375892.2:n.-199G>A
ENST00000391844.8:c.-245G>A	ENSP00000375719.4:n.-245G>A
ENST00000392038.6:c.-199G>A	ENSP00000375892.2:n.-199G>A
ENST00000424901.5:c.-199G>A	ENSP00000399532.2:n.-199G>A
ENST00000578123.5:c.-85+153G>A	ENSP00000462022.1:n.-85+153G>A
ENST00000579047.5:c.-255G>A	ENSP00000471369.1:n.-255G>A
ENST00000584288.5:c.-338G>A	ENSP00000462469.1:n.-338G>A
NM_001243027.2:c.-348G>A	NP_001229956.1:n.-348G>A
NM_001243028.2:c.-255G>A	NP_001229957.1:n.-255G>A
NM_001626.5:c.-199G>A	NP_001617.1:n.-199G>A
XM_011526620.1:c.-85+153G>A	XP_011524922.1:n.-85+153G>A
XM_011526622.1:c.-199G>A	XP_011524924.1:n.-199G>A
XM_011526622.2:c.-199G>A	XP_011524924.1:n.-199G>A
XM_024451417.1:c.-199G>A	XP_024307185.1:n.-199G>A
NM_001626.6:c.-199G>A MANE Select	NP_001617.1:n.-199G>A
NM_001243027.3:c.-348G>A	NP_001229956.1:n.-348G>A
NM_001243028.3:c.-255G>A	NP_001229957.1:n.-255G>A