Canonical Allele Identifier: CA13985957
Gene: AKT1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10149779

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104784749G>A , CM000676.2:g.104784749G>A GRCh38
NC_000014.8:g.105251086G>A , CM000676.1:g.105251086G>A GRCh37
NC_000014.7:g.104322131G>A NCBI36
NG_012188.1:g.15996C>T , LRG_721:g.15996C>T

Transcript Alleles

HGVS Amino-acid change
NM_001014431.1:c.47-4533C>T VV NP_001014431.1:p.=
NM_001014432.1:c.47-4533C>T , LRG_721t1:c.47-4533C>T NP_001014432.1:p.=
NM_005163.2:c.47-4533C>T , LRG_721t2:c.47-4533C>T NP_005154.2:p.=
XM_005267401.1:c.47-4533C>T XP_005267458.1:p.=
XM_011536543.1:c.47-4533C>T XP_011534845.1:p.=
XM_011536544.1:c.47-4533C>T XP_011534846.1:p.=
XR_002957536.1:n.247-4533C>T
ENST00000349310.7:c.47-4533C>T ENSP00000270202.4:p.=
ENST00000402615.6:c.47-4533C>T ENSP00000385326.2:p.=
ENST00000407796.6:c.47-4533C>T ENSP00000384293.2:p.=
ENST00000554581.5:c.47-4533C>T ENSP00000451828.1:p.=
ENST00000554848.5:c.47-4533C>T ENSP00000451166.1:p.=
ENST00000555380.1:n.77+1542C>T
ENST00000555528.5:c.47-4533C>T ENSP00000450688.1:p.=
ENST00000555926.1:c.47-4533C>T ENSP00000451824.1:p.=