Canonical Allele Identifier: CA405866225

Gene: AKT2

Linked Data

• MyVariant Identifiers: chr19:g.40741873T>A (hg19) ; chr19:g.40235966T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40235966T>A , CM000681.2:g.40235966T>A	GRCh38
NC_000019.9:g.40741873T>A , CM000681.1:g.40741873T>A	GRCh37
NC_000019.8:g.45433713T>A	NCBI36
NG_012038.2:g.54393A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000392038.7:c.1099A>T MANE Select	ENSP00000375892.2:p.Ile367Phe
ENST00000578615.6:c.978A>T
ENST00000311278.10:c.970A>T	ENSP00000309428.6:p.Ile324Phe
ENST00000391844.8:c.*713A>T	ENSP00000375719.4:n.*713A>T
ENST00000391845.6:n.564A>T
ENST00000392038.6:c.1099A>T	ENSP00000375892.2:p.Ile367Phe
ENST00000424901.5:c.970A>T	ENSP00000399532.2:p.Ile324Phe
ENST00000476247.6:c.106A>T	ENSP00000463368.1:p.Ile36Phe
ENST00000476266.5:n.1427A>T
ENST00000483166.5:n.2570A>T
ENST00000489375.5:c.66A>T
ENST00000496089.6:n.518A>T
ENST00000578615.5:c.667A>T	ENSP00000463262.1:p.Ile223Phe
ENST00000579047.5:c.913A>T	ENSP00000471369.1:p.Ile305Phe
ENST00000584288.5:c.*713A>T	ENSP00000462469.1:n.*713A>T
NM_001243027.2:c.913A>T	NP_001229956.1:p.Ile305Phe
NM_001243028.2:c.913A>T	NP_001229957.1:p.Ile305Phe
NM_001626.5:c.1099A>T	NP_001617.1:p.Ile367Phe
XM_011526614.1:c.1099A>T	XP_011524916.1:p.Ile367Phe
XM_011526615.1:c.1099A>T	XP_011524917.1:p.Ile367Phe
XM_011526616.1:c.1099A>T	XP_011524918.1:p.Ile367Phe
XM_011526617.1:c.1099A>T	XP_011524919.1:p.Ile367Phe
XM_011526618.1:c.1099A>T	XP_011524920.1:p.Ile367Phe
XM_011526619.1:c.1099A>T	XP_011524921.1:p.Ile367Phe
XM_011526620.1:c.1099A>T	XP_011524922.1:p.Ile367Phe
XM_011526621.1:c.1099A>T	XP_011524923.1:p.Ile367Phe
XM_011526622.1:c.1099A>T	XP_011524924.1:p.Ile367Phe
NM_001330511.1:c.970A>T	NP_001317440.1:p.Ile324Phe
XM_011526622.2:c.1099A>T	XP_011524924.1:p.Ile367Phe
XM_017026470.2:c.1099A>T	XP_016881959.1:p.Ile367Phe
XM_024451416.1:c.1099A>T	XP_024307184.1:p.Ile367Phe
XM_024451417.1:c.970A>T	XP_024307185.1:p.Ile324Phe
NM_001626.6:c.1099A>T MANE Select	NP_001617.1:p.Ile367Phe
NM_001243027.3:c.913A>T	NP_001229956.1:p.Ile305Phe
NM_001243028.3:c.913A>T	NP_001229957.1:p.Ile305Phe