Canonical Allele Identifier: CA405866217

Gene: AKT2

Linked Data

• MyVariant Identifiers: chr19:g.40741869C>G (hg19) ; chr19:g.40235962C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40235962C>G , CM000681.2:g.40235962C>G	GRCh38
NC_000019.9:g.40741869C>G , CM000681.1:g.40741869C>G	GRCh37
NC_000019.8:g.45433709C>G	NCBI36
NG_012038.2:g.54397G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000392038.7:c.1103G>C MANE Select	ENSP00000375892.2:p.Arg368Pro
ENST00000578615.6:c.982G>C
ENST00000311278.10:c.974G>C	ENSP00000309428.6:p.Arg325Pro
ENST00000391844.8:c.*717G>C	ENSP00000375719.4:n.*717G>C
ENST00000391845.6:n.568G>C
ENST00000392038.6:c.1103G>C	ENSP00000375892.2:p.Arg368Pro
ENST00000424901.5:c.974G>C	ENSP00000399532.2:p.Arg325Pro
ENST00000476247.6:c.110G>C	ENSP00000463368.1:p.Arg37Pro
ENST00000476266.5:n.1431G>C
ENST00000483166.5:n.2574G>C
ENST00000489375.5:c.70G>C
ENST00000496089.6:n.522G>C
ENST00000578615.5:c.671G>C	ENSP00000463262.1:p.Arg224Pro
ENST00000579047.5:c.917G>C	ENSP00000471369.1:p.Arg306Pro
ENST00000584288.5:c.*717G>C	ENSP00000462469.1:n.*717G>C
NM_001243027.2:c.917G>C	NP_001229956.1:p.Arg306Pro
NM_001243028.2:c.917G>C	NP_001229957.1:p.Arg306Pro
NM_001626.5:c.1103G>C	NP_001617.1:p.Arg368Pro
XM_011526614.1:c.1103G>C	XP_011524916.1:p.Arg368Pro
XM_011526615.1:c.1103G>C	XP_011524917.1:p.Arg368Pro
XM_011526616.1:c.1103G>C	XP_011524918.1:p.Arg368Pro
XM_011526617.1:c.1103G>C	XP_011524919.1:p.Arg368Pro
XM_011526618.1:c.1103G>C	XP_011524920.1:p.Arg368Pro
XM_011526619.1:c.1103G>C	XP_011524921.1:p.Arg368Pro
XM_011526620.1:c.1103G>C	XP_011524922.1:p.Arg368Pro
XM_011526621.1:c.1103G>C	XP_011524923.1:p.Arg368Pro
XM_011526622.1:c.1103G>C	XP_011524924.1:p.Arg368Pro
NM_001330511.1:c.974G>C	NP_001317440.1:p.Arg325Pro
XM_011526622.2:c.1103G>C	XP_011524924.1:p.Arg368Pro
XM_017026470.2:c.1103G>C	XP_016881959.1:p.Arg368Pro
XM_024451416.1:c.1103G>C	XP_024307184.1:p.Arg368Pro
XM_024451417.1:c.974G>C	XP_024307185.1:p.Arg325Pro
NM_001626.6:c.1103G>C MANE Select	NP_001617.1:p.Arg368Pro
NM_001243027.3:c.917G>C	NP_001229956.1:p.Arg306Pro
NM_001243028.3:c.917G>C	NP_001229957.1:p.Arg306Pro