Canonical Allele Identifier: CA405866923

Gene: AKT2

Linked Data

• dbSNP Id: rs1304063423
• gnomAD v2: 19-40743893-C-T
• MyVariant Identifiers: chr19:g.40743893C>T (hg19) ; chr19:g.40237986C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40237986C>T , CM000681.2:g.40237986C>T	GRCh38
NC_000019.9:g.40743893C>T , CM000681.1:g.40743893C>T	GRCh37
NC_000019.8:g.45435733C>T	NCBI36
NG_012038.2:g.52373G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000392038.7:c.814G>A MANE Select	ENSP00000375892.2:p.Val272Ile
ENST00000578615.6:c.693G>A
ENST00000311278.10:c.814G>A	ENSP00000309428.6:p.Val272Ile
ENST00000391844.8:c.*428G>A	ENSP00000375719.4:n.*428G>A
ENST00000391845.6:n.279G>A
ENST00000392038.6:c.814G>A	ENSP00000375892.2:p.Val272Ile
ENST00000424901.5:c.814G>A	ENSP00000399532.2:p.Val272Ile
ENST00000476266.5:n.1142G>A
ENST00000480878.6:n.241G>A
ENST00000483166.5:n.702G>A
ENST00000496089.6:n.81G>A
ENST00000578282.5:n.207G>A
ENST00000578310.1:c.75-1601G>A
ENST00000578615.5:c.382G>A	ENSP00000463262.1:p.Val128Ile
ENST00000579047.5:c.628G>A	ENSP00000471369.1:p.Val210Ile
ENST00000579345.5:n.334G>A
ENST00000580878.1:n.471G>A
ENST00000584288.5:c.*428G>A	ENSP00000462469.1:n.*428G>A
NM_001243027.2:c.628G>A	NP_001229956.1:p.Val210Ile
NM_001243028.2:c.628G>A	NP_001229957.1:p.Val210Ile
NM_001626.5:c.814G>A	NP_001617.1:p.Val272Ile
XM_011526614.1:c.814G>A	XP_011524916.1:p.Val272Ile
XM_011526615.1:c.814G>A	XP_011524917.1:p.Val272Ile
XM_011526616.1:c.814G>A	XP_011524918.1:p.Val272Ile
XM_011526617.1:c.814G>A	XP_011524919.1:p.Val272Ile
XM_011526618.1:c.814G>A	XP_011524920.1:p.Val272Ile
XM_011526619.1:c.814G>A	XP_011524921.1:p.Val272Ile
XM_011526620.1:c.814G>A	XP_011524922.1:p.Val272Ile
XM_011526621.1:c.814G>A	XP_011524923.1:p.Val272Ile
XM_011526622.1:c.814G>A	XP_011524924.1:p.Val272Ile
NM_001330511.1:c.814G>A	NP_001317440.1:p.Val272Ile
XM_011526622.2:c.814G>A	XP_011524924.1:p.Val272Ile
XM_017026470.2:c.814G>A	XP_016881959.1:p.Val272Ile
XM_024451416.1:c.814G>A	XP_024307184.1:p.Val272Ile
XM_024451417.1:c.814G>A	XP_024307185.1:p.Val272Ile
NM_001626.6:c.814G>A MANE Select	NP_001617.1:p.Val272Ile
NM_001243027.3:c.628G>A	NP_001229956.1:p.Val210Ile
NM_001243028.3:c.628G>A	NP_001229957.1:p.Val210Ile