Canonical Allele Identifier: CA345669813
Gene: AKT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.243637685T>A , CM000663.2:g.243637685T>A GRCh38
NC_000001.10:g.243800987T>A , CM000663.1:g.243800987T>A GRCh37
NC_000001.9:g.241867610T>A NCBI36
NG_029764.1:g.210900A>T
NG_029764.2:g.218395A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263826.12:c.487A>T ENSP00000263826.5:p.Ile163Phe
ENST00000366539.6:c.487A>T ENSP00000355497.2:p.Ile163Phe
ENST00000492957.2:c.487A>T ENSP00000506695.1:p.Ile163Phe
ENST00000672460.1:c.244A>T ENSP00000499842.1:p.Ile82Phe
ENST00000672578.1:c.304A>T ENSP00000500597.1:p.Ile102Phe
ENST00000673466.1:c.487A>T MANE Select ENSP00000500582.1:p.Ile163Phe
ENST00000680056.1:c.361A>T ENSP00000505337.1:p.Ile121Phe
ENST00000680118.1:c.487A>T ENSP00000505276.1:p.Ile163Phe
ENST00000681794.1:c.487A>T ENSP00000506399.1:p.Ile163Phe
ENST00000263826.9:c.487A>T ENSP00000263826.5:p.Ile163Phe
ENST00000336199.9:c.487A>T ENSP00000336943.5:p.Ile163Phe
ENST00000366539.5:c.487A>T ENSP00000355497.1:p.Ile163Phe
ENST00000366540.5:c.487A>T ENSP00000355498.1:p.Ile163Phe
NM_001206729.1:c.487A>T NP_001193658.1:p.Ile163Phe
NM_005465.4:c.487A>T NP_005456.1:p.Ile163Phe
NM_181690.2:c.487A>T NP_859029.1:p.Ile163Phe
XM_005272994.3:c.487A>T XP_005273051.1:p.Ile163Phe
XM_005272995.2:c.487A>T XP_005273052.1:p.Ile163Phe
XM_005272997.3:c.304A>T XP_005273054.1:p.Ile102Phe
XM_006711726.2:c.487A>T XP_006711789.1:p.Ile163Phe
XM_011544011.1:c.361A>T XP_011542313.1:p.Ile121Phe
XM_011544012.1:c.487A>T XP_011542314.1:p.Ile163Phe
XM_011544013.1:c.487A>T XP_011542315.1:p.Ile163Phe
XM_016999985.1:c.304A>T XP_016855474.1:p.Ile102Phe
XM_024446000.1:c.487A>T XP_024301768.1:p.Ile163Phe
XM_024446892.1:c.487A>T XP_024302660.1:p.Ile163Phe
XM_024447938.1:c.487A>T XP_024303706.1:p.Ile163Phe
NM_005465.5:c.487A>T NP_005456.1:p.Ile163Phe
NM_001370074.1:c.487A>T NP_001357003.1:p.Ile163Phe
NM_005465.7:c.487A>T MANE Select NP_005456.1:p.Ile163Phe
NM_001206729.2:c.487A>T NP_001193658.1:p.Ile163Phe