Canonical Allele Identifier: CA2585108903

Gene: AKT2

Linked Data

• gnomAD v4: 19-40285298-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285298C>A , CM000681.2:g.40285298C>A	GRCh38
NC_000019.9:g.40791205C>A , CM000681.1:g.40791205C>A	GRCh37
NC_000019.8:g.45483045C>A	NCBI36
NG_012038.2:g.5061G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-202G>T MANE Select	ENSP00000375892.2:n.-202G>T
ENST00000391844.8:c.-248G>T	ENSP00000375719.4:n.-248G>T
ENST00000392038.6:c.-202G>T	ENSP00000375892.2:n.-202G>T
ENST00000424901.5:c.-202G>T	ENSP00000399532.2:n.-202G>T
ENST00000578123.5:c.-85+150G>T	ENSP00000462022.1:n.-85+150G>T
ENST00000579047.5:c.-258G>T	ENSP00000471369.1:n.-258G>T
ENST00000584288.5:c.-341G>T	ENSP00000462469.1:n.-341G>T
NM_001243027.2:c.-351G>T	NP_001229956.1:n.-351G>T
NM_001243028.2:c.-258G>T	NP_001229957.1:n.-258G>T
NM_001626.5:c.-202G>T	NP_001617.1:n.-202G>T
XM_011526620.1:c.-85+150G>T	XP_011524922.1:n.-85+150G>T
XM_011526622.1:c.-202G>T	XP_011524924.1:n.-202G>T
XM_011526622.2:c.-202G>T	XP_011524924.1:n.-202G>T
XM_024451417.1:c.-202G>T	XP_024307185.1:n.-202G>T
NM_001626.6:c.-202G>T MANE Select	NP_001617.1:n.-202G>T
NM_001243027.3:c.-351G>T	NP_001229956.1:n.-351G>T
NM_001243028.3:c.-258G>T	NP_001229957.1:n.-258G>T