Canonical Allele Identifier: CA507483815

Gene: AKT2

Linked Data

• dbSNP Id: rs2145177911
• gnomAD v4: 19-40237981-G-A
• MyVariant Identifiers: chr19:g.40743888G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40237981G>A , CM000681.2:g.40237981G>A	GRCh38
NC_000019.9:g.40743888G>A , CM000681.1:g.40743888G>A	GRCh37
NC_000019.8:g.45435728G>A	NCBI36
NG_012038.2:g.52378C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000392038.7:c.819C>T MANE Select	ENSP00000375892.2:p.Tyr273=
ENST00000578615.6:c.698C>T
ENST00000311278.10:c.819C>T	ENSP00000309428.6:p.Tyr273=
ENST00000391844.8:c.*433C>T	ENSP00000375719.4:n.*433C>T
ENST00000391845.6:n.284C>T
ENST00000392038.6:c.819C>T	ENSP00000375892.2:p.Tyr273=
ENST00000424901.5:c.819C>T	ENSP00000399532.2:p.Tyr273=
ENST00000476266.5:n.1147C>T
ENST00000480878.6:n.246C>T
ENST00000483166.5:n.707C>T
ENST00000496089.6:n.86C>T
ENST00000578282.5:n.212C>T
ENST00000578310.1:c.75-1596C>T
ENST00000578615.5:c.387C>T	ENSP00000463262.1:p.Tyr129=
ENST00000579047.5:c.633C>T	ENSP00000471369.1:p.Tyr211=
ENST00000579345.5:n.339C>T
ENST00000580878.1:n.476C>T
ENST00000584288.5:c.*433C>T	ENSP00000462469.1:n.*433C>T
NM_001243027.2:c.633C>T	NP_001229956.1:p.Tyr211=
NM_001243028.2:c.633C>T	NP_001229957.1:p.Tyr211=
NM_001626.5:c.819C>T	NP_001617.1:p.Tyr273=
XM_011526614.1:c.819C>T	XP_011524916.1:p.Tyr273=
XM_011526615.1:c.819C>T	XP_011524917.1:p.Tyr273=
XM_011526616.1:c.819C>T	XP_011524918.1:p.Tyr273=
XM_011526617.1:c.819C>T	XP_011524919.1:p.Tyr273=
XM_011526618.1:c.819C>T	XP_011524920.1:p.Tyr273=
XM_011526619.1:c.819C>T	XP_011524921.1:p.Tyr273=
XM_011526620.1:c.819C>T	XP_011524922.1:p.Tyr273=
XM_011526621.1:c.819C>T	XP_011524923.1:p.Tyr273=
XM_011526622.1:c.819C>T	XP_011524924.1:p.Tyr273=
NM_001330511.1:c.819C>T	NP_001317440.1:p.Tyr273=
XM_011526622.2:c.819C>T	XP_011524924.1:p.Tyr273=
XM_017026470.2:c.819C>T	XP_016881959.1:p.Tyr273=
XM_024451416.1:c.819C>T	XP_024307184.1:p.Tyr273=
XM_024451417.1:c.819C>T	XP_024307185.1:p.Tyr273=
NM_001626.6:c.819C>T MANE Select	NP_001617.1:p.Tyr273=
NM_001243027.3:c.633C>T	NP_001229956.1:p.Tyr211=
NM_001243028.3:c.633C>T	NP_001229957.1:p.Tyr211=