Canonical Allele Identifier: CA2160960526

Gene: AKT1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104770755T= , CM000676.2:g.104770755T=	GRCh38
NC_000014.8:g.105237092T= , CM000676.1:g.105237092T=	GRCh37
NC_000014.7:g.104308137T=	NCBI36
NG_012188.1:g.29990A= , LRG_721:g.29990A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554192.6:c.1254A=	ENSP00000450681.3:p.Pro418=
ENST00000554585.6:c.*179A=	ENSP00000481526.2:n.*179A=
ENST00000555458.6:c.1353A=	ENSP00000451470.3:p.Pro451=
ENST00000553797.2:c.1428A=	ENSP00000507566.1:p.Pro476=
ENST00000554826.2:n.1822A=
ENST00000610370.2:n.3339A=
ENST00000683058.1:n.1230A=
ENST00000683722.1:c.1353A=	ENSP00000507879.1:p.Pro451=
ENST00000684058.1:n.910A=
ENST00000407796.7:c.1353A=	ENSP00000384293.2:p.Pro451=
ENST00000649815.2:c.1353A= MANE Select	ENSP00000497822.1:p.Pro451=
ENST00000349310.7:c.1353A=	ENSP00000270202.4:p.Pro451=
ENST00000402615.6:c.1353A=	ENSP00000385326.2:p.Pro451=
ENST00000407796.6:c.1353A=	ENSP00000384293.2:p.Pro451=
ENST00000544168.5:n.1288A=
ENST00000553506.5:n.1751A=
ENST00000554192.5:c.463A=
ENST00000554581.5:c.1353A=	ENSP00000451828.1:p.Pro451=
ENST00000554585.5:c.620A=	ENSP00000481526.1:n.620A=
ENST00000554848.5:c.1353A=	ENSP00000451166.1:p.Pro451=
ENST00000555458.5:c.460A=
ENST00000555528.5:c.1353A=	ENSP00000450688.1:p.Pro451=
ENST00000557552.1:n.7317A=
ENST00000610370.1:n.1784A=
NM_001014431.1:c.1353A=	NP_001014431.1:p.Pro451=
NM_001014432.1:c.1353A= , LRG_721t1:c.1353A=	NP_001014432.1:p.Pro451=
NM_005163.2:c.1353A= , LRG_721t2:c.1353A=	NP_005154.2:p.Pro451=
XM_005267401.1:c.1353A=	XP_005267458.1:p.Pro451=
XM_011536543.1:c.1353A=	XP_011534845.1:p.Pro451=
XR_002957536.1:n.3070A=
NM_001014431.2:c.1353A=	NP_001014431.1:p.Pro451=
NM_001014432.2:c.1353A=	NP_001014432.1:p.Pro451=
NM_001382430.1:c.1353A= MANE Select	NP_001369359.1:p.Pro451=
NM_001382431.1:c.1353A=	NP_001369360.1:p.Pro451=
NM_001382432.1:c.1353A=	NP_001369361.1:p.Pro451=
NM_001382433.1:c.1353A=	NP_001369362.1:p.Pro451=