Canonical Allele Identifier: CA9441674

Gene: AKT2

Linked Data

• ClinVar Variation Id: 2926089
• ClinVar RCV Id: RCV003786375
• dbSNP Id: rs758906645
• ExAC: 19:40743885 G / C
• gnomAD v2: 19-40743885-G-C
• gnomAD v3: 19-40237978-G-C
• gnomAD v4: 19-40237978-G-C
• MyVariant Identifiers: chr19:g.40743885G>C (hg19) ; chr19:g.40237978G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40237978G>C , CM000681.2:g.40237978G>C	GRCh38
NC_000019.9:g.40743885G>C , CM000681.1:g.40743885G>C	GRCh37
NC_000019.8:g.45435725G>C	NCBI36
NG_012038.2:g.52381C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.822C>G MANE Select	ENSP00000375892.2:p.Arg274=
ENST00000578615.6:c.701C>G
ENST00000311278.10:c.822C>G	ENSP00000309428.6:p.Arg274=
ENST00000391844.8:c.*436C>G	ENSP00000375719.4:n.*436C>G
ENST00000391845.6:n.287C>G
ENST00000392038.6:c.822C>G	ENSP00000375892.2:p.Arg274=
ENST00000424901.5:c.822C>G	ENSP00000399532.2:p.Arg274=
ENST00000476266.5:n.1150C>G
ENST00000480878.6:n.249C>G
ENST00000483166.5:n.710C>G
ENST00000496089.6:n.89C>G
ENST00000578282.5:n.215C>G
ENST00000578310.1:c.75-1593C>G
ENST00000578615.5:c.390C>G	ENSP00000463262.1:p.Arg130=
ENST00000579047.5:c.636C>G	ENSP00000471369.1:p.Arg212=
ENST00000579345.5:n.342C>G
ENST00000580878.1:n.479C>G
ENST00000584288.5:c.*436C>G	ENSP00000462469.1:n.*436C>G
NM_001243027.2:c.636C>G	NP_001229956.1:p.Arg212=
NM_001243028.2:c.636C>G	NP_001229957.1:p.Arg212=
NM_001626.5:c.822C>G	NP_001617.1:p.Arg274=
XM_011526614.1:c.822C>G	XP_011524916.1:p.Arg274=
XM_011526615.1:c.822C>G	XP_011524917.1:p.Arg274=
XM_011526616.1:c.822C>G	XP_011524918.1:p.Arg274=
XM_011526617.1:c.822C>G	XP_011524919.1:p.Arg274=
XM_011526618.1:c.822C>G	XP_011524920.1:p.Arg274=
XM_011526619.1:c.822C>G	XP_011524921.1:p.Arg274=
XM_011526620.1:c.822C>G	XP_011524922.1:p.Arg274=
XM_011526621.1:c.822C>G	XP_011524923.1:p.Arg274=
XM_011526622.1:c.822C>G	XP_011524924.1:p.Arg274=
NM_001330511.1:c.822C>G	NP_001317440.1:p.Arg274=
XM_011526622.2:c.822C>G	XP_011524924.1:p.Arg274=
XM_017026470.2:c.822C>G	XP_016881959.1:p.Arg274=
XM_024451416.1:c.822C>G	XP_024307184.1:p.Arg274=
XM_024451417.1:c.822C>G	XP_024307185.1:p.Arg274=
NM_001626.6:c.822C>G MANE Select	NP_001617.1:p.Arg274=
NM_001243027.3:c.636C>G	NP_001229956.1:p.Arg212=
NM_001243028.3:c.636C>G	NP_001229957.1:p.Arg212=