Canonical Allele Identifier: CA2585108825

Gene: AKT2

Linked Data

• gnomAD v4: 19-40285218-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285218C>A , CM000681.2:g.40285218C>A	GRCh38
NC_000019.9:g.40791125C>A , CM000681.1:g.40791125C>A	GRCh37
NC_000019.8:g.45482965C>A	NCBI36
NG_012038.2:g.5141G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-122G>T MANE Select	ENSP00000375892.2:n.-122G>T
ENST00000358335.9:c.-122G>T	ENSP00000351095.5:n.-122G>T
ENST00000391844.8:c.-168G>T	ENSP00000375719.4:n.-168G>T
ENST00000392038.6:c.-122G>T	ENSP00000375892.2:n.-122G>T
ENST00000424901.5:c.-122G>T	ENSP00000399532.2:n.-122G>T
ENST00000578123.5:c.-85+230G>T	ENSP00000462022.1:n.-85+230G>T
ENST00000579047.5:c.-178G>T	ENSP00000471369.1:n.-178G>T
ENST00000584288.5:c.-261G>T	ENSP00000462469.1:n.-261G>T
NM_001243027.2:c.-271G>T	NP_001229956.1:n.-271G>T
NM_001243028.2:c.-178G>T	NP_001229957.1:n.-178G>T
NM_001626.5:c.-122G>T	NP_001617.1:n.-122G>T
XM_011526620.1:c.-85+230G>T	XP_011524922.1:n.-85+230G>T
XM_011526622.1:c.-122G>T	XP_011524924.1:n.-122G>T
XM_011526622.2:c.-122G>T	XP_011524924.1:n.-122G>T
XM_024451417.1:c.-122G>T	XP_024307185.1:n.-122G>T
NM_001626.6:c.-122G>T MANE Select	NP_001617.1:n.-122G>T
NM_001243027.3:c.-271G>T	NP_001229956.1:n.-271G>T
NM_001243028.3:c.-178G>T	NP_001229957.1:n.-178G>T