Canonical Allele Identifier: CA130584

Gene: AKT3

Linked Data

• ClinVar Variation Id: 39816
• ClinVar RCV Id: RCV000033037 ; RCV001836719
• dbSNP Id: rs397514606
• COSMIC: COSM224779 ; COSM1134859 ; COSM1134860
• MyVariant Identifiers: chr1:g.243859016C>T (hg19) ; chr1:g.243695714C>T (hg38)
• CIViC: CA130584
• PubMed: PMID:22500628 ; PMID:22729223
• ERepo: CA130584/MONDO:0016054/018 ; CA130584/MONDO:0100283/018

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243695714C>T , CM000663.2:g.243695714C>T	GRCh38
NC_000001.10:g.243859016C>T , CM000663.1:g.243859016C>T	GRCh37
NC_000001.9:g.241925639C>T	NCBI36
NG_029764.1:g.152871G>A
NG_029764.2:g.160366G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263826.12:c.49G>A	ENSP00000263826.5:p.Glu17Lys
ENST00000366539.6:c.49G>A	ENSP00000355497.2:p.Glu17Lys
ENST00000491219.6:c.43G>A	ENSP00000499914.1:p.Glu15Lys
ENST00000492957.2:c.49G>A	ENSP00000506695.1:p.Glu17Lys
ENST00000552631.2:n.163G>A
ENST00000672238.1:c.49G>A	ENSP00000506535.1:p.Glu17Lys
ENST00000672442.1:c.49G>A	ENSP00000500134.1:p.Glu17Lys
ENST00000672578.1:c.-135G>A	ENSP00000500597.1:n.-135G>A
ENST00000672679.1:n.6G>A
ENST00000673400.1:c.49G>A	ENSP00000504988.1:p.Glu17Lys
ENST00000673466.1:c.49G>A MANE Select	ENSP00000500582.1:p.Glu17Lys
ENST00000680056.1:c.47-30831G>A	ENSP00000505337.1:n.47-30831G>A
ENST00000680118.1:c.49G>A	ENSP00000505276.1:p.Glu17Lys
ENST00000681794.1:c.49G>A	ENSP00000506399.1:p.Glu17Lys
ENST00000263826.9:c.49G>A	ENSP00000263826.5:p.Glu17Lys
ENST00000336199.9:c.49G>A	ENSP00000336943.5:p.Glu17Lys
ENST00000366539.5:c.49G>A	ENSP00000355497.1:p.Glu17Lys
ENST00000366540.5:c.49G>A	ENSP00000355498.1:p.Glu17Lys
ENST00000463991.5:n.187G>A
ENST00000490018.1:n.541G>A
ENST00000491219.5:n.3G>A
ENST00000552631.1:c.49G>A	ENSP00000447820.1:p.Glu17Lys
NM_001206729.1:c.49G>A	NP_001193658.1:p.Glu17Lys
NM_005465.4:c.49G>A	NP_005456.1:p.Glu17Lys
NM_181690.2:c.49G>A	NP_859029.1:p.Glu17Lys
XM_005272994.3:c.49G>A	XP_005273051.1:p.Glu17Lys
XM_005272995.2:c.49G>A	XP_005273052.1:p.Glu17Lys
XM_006711726.2:c.49G>A	XP_006711789.1:p.Glu17Lys
XM_011544011.1:c.47-30831G>A	XP_011542313.1:n.47-30831G>A
XM_011544012.1:c.49G>A	XP_011542314.1:p.Glu17Lys
XM_011544013.1:c.49G>A	XP_011542315.1:p.Glu17Lys
XM_016999985.1:c.-249G>A	XP_016855474.1:n.-249G>A
XM_024446000.1:c.49G>A	XP_024301768.1:p.Glu17Lys
XM_024446892.1:c.49G>A	XP_024302660.1:p.Glu17Lys
XM_024447938.1:c.49G>A	XP_024303706.1:p.Glu17Lys
NM_005465.5:c.49G>A	NP_005456.1:p.Glu17Lys
NM_001370074.1:c.49G>A	NP_001357003.1:p.Glu17Lys
NM_005465.7:c.49G>A MANE Select	NP_005456.1:p.Glu17Lys
NM_001206729.2:c.49G>A	NP_001193658.1:p.Glu17Lys