Canonical Allele Identifier: CA2160973203
Gene: AKT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104793309G= , CM000676.2:g.104793309G= GRCh38
NC_000014.8:g.105259646G= , CM000676.1:g.105259646G= GRCh37
NC_000014.7:g.104330691G= NCBI36
NG_012188.1:g.7436C= , LRG_721:g.7436C=

Transcript Alleles

HGVS Amino-acid change
ENST00000554192.6:c.-79-587C= ENSP00000450681.3:n.-79-587C=
ENST00000554585.6:c.-79-587C= ENSP00000481526.2:n.-79-587C=
ENST00000555458.6:c.-79-587C= ENSP00000451470.3:n.-79-587C=
ENST00000553797.2:c.-262C= ENSP00000507566.1:n.-262C=
ENST00000554826.2:n.60-587C=
ENST00000610370.2:n.60-587C=
ENST00000682269.1:n.261-5C=
ENST00000683722.1:c.-79-587C= ENSP00000507879.1:n.-79-587C=
ENST00000407796.7:c.-79-587C= ENSP00000384293.2:n.-79-587C=
ENST00000649815.2:c.-257-5C= MANE Select ENSP00000497822.1:n.-257-5C=
ENST00000349310.7:c.-163-99C= ENSP00000270202.4:n.-163-99C=
ENST00000402615.6:c.-262C= ENSP00000385326.2:n.-262C=
ENST00000407796.6:c.-79-587C= ENSP00000384293.2:n.-79-587C=
ENST00000554581.5:c.-666C= ENSP00000451828.1:n.-666C=
ENST00000554848.5:c.-79-587C= ENSP00000451166.1:n.-79-587C=
ENST00000555528.5:c.-262C= ENSP00000450688.1:n.-262C=
ENST00000555926.1:c.-257-5C= ENSP00000451824.1:n.-257-5C=
ENST00000557494.1:n.261-5C=
NM_001014431.1:c.-79-587C= NP_001014431.1:n.-79-587C=
NM_001014432.1:c.-163-99C= , LRG_721t1:c.-163-99C= NP_001014432.1:n.-163-99C=
NM_005163.2:c.-262C= , LRG_721t2:c.-262C= NP_005154.2:n.-262C=
XM_005267401.1:c.-79-587C= XP_005267458.1:n.-79-587C=
XM_011536543.1:c.-257-5C= XP_011534845.1:n.-257-5C=
XM_011536544.1:c.-262C= XP_011534846.1:n.-262C=
XR_002957536.1:n.38-99C=
NM_001014431.2:c.-79-587C= NP_001014431.1:n.-79-587C=
NM_001014432.2:c.-163-99C= NP_001014432.1:n.-163-99C=
NM_001382430.1:c.-257-5C= MANE Select NP_001369359.1:n.-257-5C=
NM_001382431.1:c.-79-587C= NP_001369360.1:n.-79-587C=
NM_001382432.1:c.-163-99C= NP_001369361.1:n.-163-99C=
NM_001382433.1:c.-257-5C= NP_001369362.1:n.-257-5C=