Canonical Allele Identifier: CA507483861

Gene: AKT2

Linked Data

• gnomAD v4: 19-40238047-C-A
• MyVariant Identifiers: chr19:g.40743954C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40238047C>A , CM000681.2:g.40238047C>A	GRCh38
NC_000019.9:g.40743954C>A , CM000681.1:g.40743954C>A	GRCh37
NC_000019.8:g.45435794C>A	NCBI36
NG_012038.2:g.52312G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.753G>T MANE Select	ENSP00000375892.2:p.Arg251=
ENST00000578615.6:c.632G>T
ENST00000311278.10:c.753G>T	ENSP00000309428.6:p.Arg251=
ENST00000391844.8:c.*367G>T	ENSP00000375719.4:n.*367G>T
ENST00000391845.6:n.218G>T
ENST00000392038.6:c.753G>T	ENSP00000375892.2:p.Arg251=
ENST00000424901.5:c.753G>T	ENSP00000399532.2:p.Arg251=
ENST00000476266.5:n.1081G>T
ENST00000480878.6:n.180G>T
ENST00000483166.5:n.641G>T
ENST00000496089.6:n.20G>T
ENST00000578282.5:n.146G>T
ENST00000578310.1:c.75-1662G>T
ENST00000578615.5:c.321G>T	ENSP00000463262.1:p.Arg107=
ENST00000579047.5:c.567G>T	ENSP00000471369.1:p.Arg189=
ENST00000579345.5:n.273G>T
ENST00000580878.1:n.410G>T
ENST00000584288.5:c.*367G>T	ENSP00000462469.1:n.*367G>T
ENST00000601166.5:c.497G>T	ENSP00000472371.1:n.497G>T
NM_001243027.2:c.567G>T	NP_001229956.1:p.Arg189=
NM_001243028.2:c.567G>T	NP_001229957.1:p.Arg189=
NM_001626.5:c.753G>T	NP_001617.1:p.Arg251=
XM_011526614.1:c.753G>T	XP_011524916.1:p.Arg251=
XM_011526615.1:c.753G>T	XP_011524917.1:p.Arg251=
XM_011526616.1:c.753G>T	XP_011524918.1:p.Arg251=
XM_011526617.1:c.753G>T	XP_011524919.1:p.Arg251=
XM_011526618.1:c.753G>T	XP_011524920.1:p.Arg251=
XM_011526619.1:c.753G>T	XP_011524921.1:p.Arg251=
XM_011526620.1:c.753G>T	XP_011524922.1:p.Arg251=
XM_011526621.1:c.753G>T	XP_011524923.1:p.Arg251=
XM_011526622.1:c.753G>T	XP_011524924.1:p.Arg251=
NM_001330511.1:c.753G>T	NP_001317440.1:p.Arg251=
XM_011526622.2:c.753G>T	XP_011524924.1:p.Arg251=
XM_017026470.2:c.753G>T	XP_016881959.1:p.Arg251=
XM_024451416.1:c.753G>T	XP_024307184.1:p.Arg251=
XM_024451417.1:c.753G>T	XP_024307185.1:p.Arg251=
NM_001626.6:c.753G>T MANE Select	NP_001617.1:p.Arg251=
NM_001243027.3:c.567G>T	NP_001229956.1:p.Arg189=
NM_001243028.3:c.567G>T	NP_001229957.1:p.Arg189=