Canonical Allele Identifier: CA391214398
Gene: AKT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104770750T>G , CM000676.2:g.104770750T>G GRCh38
NC_000014.8:g.105237087T>G , CM000676.1:g.105237087T>G GRCh37
NC_000014.7:g.104308132T>G NCBI36
NG_012188.1:g.29995A>C , LRG_721:g.29995A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000554192.6:c.1259A>C ENSP00000450681.3:p.Asp420Ala
ENST00000554585.6:c.*184A>C ENSP00000481526.2:n.*184A>C
ENST00000555458.6:c.1358A>C ENSP00000451470.3:p.Asp453Ala
ENST00000553797.2:c.1433A>C ENSP00000507566.1:p.Asp478Ala
ENST00000554826.2:n.1827A>C
ENST00000610370.2:n.3344A>C
ENST00000683058.1:n.1235A>C
ENST00000683722.1:c.1358A>C ENSP00000507879.1:p.Asp453Ala
ENST00000684058.1:n.915A>C
ENST00000407796.7:c.1358A>C ENSP00000384293.2:p.Asp453Ala
ENST00000649815.2:c.1358A>C MANE Select ENSP00000497822.1:p.Asp453Ala
ENST00000349310.7:c.1358A>C ENSP00000270202.4:p.Asp453Ala
ENST00000402615.6:c.1358A>C ENSP00000385326.2:p.Asp453Ala
ENST00000407796.6:c.1358A>C ENSP00000384293.2:p.Asp453Ala
ENST00000544168.5:n.1293A>C
ENST00000553506.5:n.1756A>C
ENST00000554192.5:c.468A>C
ENST00000554581.5:c.1358A>C ENSP00000451828.1:p.Asp453Ala
ENST00000554585.5:c.625A>C ENSP00000481526.1:n.625A>C
ENST00000554848.5:c.1358A>C ENSP00000451166.1:p.Asp453Ala
ENST00000555458.5:c.465A>C
ENST00000555528.5:c.1358A>C ENSP00000450688.1:p.Asp453Ala
ENST00000557552.1:n.7322A>C
ENST00000610370.1:n.1789A>C
NM_001014431.1:c.1358A>C NP_001014431.1:p.Asp453Ala
NM_001014432.1:c.1358A>C , LRG_721t1:c.1358A>C NP_001014432.1:p.Asp453Ala
NM_005163.2:c.1358A>C , LRG_721t2:c.1358A>C NP_005154.2:p.Asp453Ala
XM_005267401.1:c.1358A>C XP_005267458.1:p.Asp453Ala
XM_011536543.1:c.1358A>C XP_011534845.1:p.Asp453Ala
XR_002957536.1:n.3075A>C
NM_001014431.2:c.1358A>C NP_001014431.1:p.Asp453Ala
NM_001014432.2:c.1358A>C NP_001014432.1:p.Asp453Ala
NM_001382430.1:c.1358A>C MANE Select NP_001369359.1:p.Asp453Ala
NM_001382431.1:c.1358A>C NP_001369360.1:p.Asp453Ala
NM_001382432.1:c.1358A>C NP_001369361.1:p.Asp453Ala
NM_001382433.1:c.1358A>C NP_001369362.1:p.Asp453Ala