Canonical Allele Identifier: CA10961483

Gene: AKT3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243779782C>A , CM000663.2:g.243779782C>A	GRCh38
NC_000001.10:g.243943084C>A , CM000663.1:g.243943084C>A	GRCh37
NC_000001.9:g.242009707C>A	NCBI36
NG_029764.1:g.68803G>T
NG_029764.2:g.76298G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263826.12:c.46+63343G>T	ENSP00000263826.5:n.46+63343G>T
ENST00000366539.6:c.46+63343G>T	ENSP00000355497.2:n.46+63343G>T
ENST00000491219.6:c.40+63343G>T	ENSP00000499914.1:n.40+63343G>T
ENST00000492957.2:c.46+63343G>T	ENSP00000506695.1:n.46+63343G>T
ENST00000552631.2:n.160+63343G>T
ENST00000672238.1:c.46+63343G>T	ENSP00000506535.1:n.46+63343G>T
ENST00000672442.1:c.46+63343G>T	ENSP00000500134.1:n.46+63343G>T
ENST00000672578.1:c.-138+70258G>T	ENSP00000500597.1:n.-138+70258G>T
ENST00000672679.1:n.3+63343G>T
ENST00000673400.1:c.46+63343G>T	ENSP00000504988.1:n.46+63343G>T
ENST00000673466.1:c.46+63343G>T MANE Select	ENSP00000500582.1:n.46+63343G>T
ENST00000680056.1:c.46+63343G>T	ENSP00000505337.1:n.46+63343G>T
ENST00000680118.1:c.46+63343G>T	ENSP00000505276.1:n.46+63343G>T
ENST00000681794.1:c.46+63343G>T	ENSP00000506399.1:n.46+63343G>T
ENST00000263826.9:c.46+63343G>T	ENSP00000263826.5:n.46+63343G>T
ENST00000336199.9:c.46+63343G>T	ENSP00000336943.5:n.46+63343G>T
ENST00000366539.5:c.46+63343G>T	ENSP00000355497.1:n.46+63343G>T
ENST00000366540.5:c.46+63343G>T	ENSP00000355498.1:n.46+63343G>T
ENST00000463991.5:n.184+34717G>T
ENST00000490018.1:n.238+28341G>T
ENST00000550388.1:n.357+8920G>T
ENST00000552631.1:c.46+63343G>T	ENSP00000447820.1:n.46+63343G>T
NM_001206729.1:c.46+63343G>T	NP_001193658.1:n.46+63343G>T
NM_005465.4:c.46+63343G>T	NP_005456.1:n.46+63343G>T
NM_181690.2:c.46+63343G>T	NP_859029.1:n.46+63343G>T
XM_005272994.3:c.46+63343G>T	XP_005273051.1:n.46+63343G>T
XM_005272995.2:c.46+63343G>T	XP_005273052.1:n.46+63343G>T
XM_006711726.2:c.46+63343G>T	XP_006711789.1:n.46+63343G>T
XM_011544011.1:c.46+63343G>T	XP_011542313.1:n.46+63343G>T
XM_011544012.1:c.46+63343G>T	XP_011542314.1:n.46+63343G>T
XM_011544013.1:c.46+63343G>T	XP_011542315.1:n.46+63343G>T
XM_016999985.1:c.-252+63343G>T	XP_016855474.1:n.-252+63343G>T
XM_024446000.1:c.46+63343G>T	XP_024301768.1:n.46+63343G>T
XM_024446892.1:c.46+63343G>T	XP_024302660.1:n.46+63343G>T
XM_024447938.1:c.46+63343G>T	XP_024303706.1:n.46+63343G>T
NM_005465.5:c.46+63343G>T	NP_005456.1:n.46+63343G>T
NM_001370074.1:c.46+63343G>T	NP_001357003.1:n.46+63343G>T
NM_005465.7:c.46+63343G>T MANE Select	NP_005456.1:n.46+63343G>T
NM_001206729.2:c.46+63343G>T	NP_001193658.1:n.46+63343G>T