Canonical Allele Identifier: CA1230495514

Gene: AKT3

Linked Data

• dbSNP Id: rs1572144593

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243671798G>C , CM000663.2:g.243671798G>C	GRCh38
NC_000001.10:g.243835100G>C , CM000663.1:g.243835100G>C	GRCh37
NC_000001.9:g.241901723G>C	NCBI36
NG_029764.1:g.176787C>G
NG_029764.2:g.184282C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263826.12:c.173-6915C>G	ENSP00000263826.5:n.173-6915C>G
ENST00000366539.6:c.173-6915C>G	ENSP00000355497.2:n.173-6915C>G
ENST00000492957.2:c.173-6915C>G	ENSP00000506695.1:n.173-6915C>G
ENST00000552631.2:n.287-6915C>G
ENST00000672238.1:c.173-6915C>G	ENSP00000506535.1:n.173-6915C>G
ENST00000672442.1:c.*2-6915C>G	ENSP00000500134.1:n.*2-6915C>G
ENST00000672578.1:c.-11-6915C>G	ENSP00000500597.1:n.-11-6915C>G
ENST00000672679.1:n.130-6915C>G
ENST00000673466.1:c.173-6915C>G MANE Select	ENSP00000500582.1:n.173-6915C>G
ENST00000680056.1:c.47-6915C>G	ENSP00000505337.1:n.47-6915C>G
ENST00000680118.1:c.173-6915C>G	ENSP00000505276.1:n.173-6915C>G
ENST00000681794.1:c.173-6915C>G	ENSP00000506399.1:n.173-6915C>G
ENST00000263826.9:c.173-6915C>G	ENSP00000263826.5:n.173-6915C>G
ENST00000336199.9:c.173-6915C>G	ENSP00000336943.5:n.173-6915C>G
ENST00000366539.5:c.173-6915C>G	ENSP00000355497.1:n.173-6915C>G
ENST00000366540.5:c.173-6915C>G	ENSP00000355498.1:n.173-6915C>G
ENST00000463991.5:n.311-6915C>G
ENST00000552631.1:c.173-6915C>G	ENSP00000447820.1:n.173-6915C>G
NM_001206729.1:c.173-6915C>G	NP_001193658.1:n.173-6915C>G
NM_005465.4:c.173-6915C>G	NP_005456.1:n.173-6915C>G
NM_181690.2:c.173-6915C>G	NP_859029.1:n.173-6915C>G
XM_005272994.3:c.173-6915C>G	XP_005273051.1:n.173-6915C>G
XM_005272995.2:c.173-6915C>G	XP_005273052.1:n.173-6915C>G
XM_005272997.3:c.-11-6915C>G	XP_005273054.1:n.-11-6915C>G
XM_006711726.2:c.173-6915C>G	XP_006711789.1:n.173-6915C>G
XM_011544011.1:c.47-6915C>G	XP_011542313.1:n.47-6915C>G
XM_011544012.1:c.173-6915C>G	XP_011542314.1:n.173-6915C>G
XM_011544013.1:c.173-6915C>G	XP_011542315.1:n.173-6915C>G
XM_016999985.1:c.-11-6915C>G	XP_016855474.1:n.-11-6915C>G
XM_024446000.1:c.173-6915C>G	XP_024301768.1:n.173-6915C>G
XM_024446892.1:c.173-6915C>G	XP_024302660.1:n.173-6915C>G
XM_024447938.1:c.173-6915C>G	XP_024303706.1:n.173-6915C>G
NM_005465.5:c.173-6915C>G	NP_005456.1:n.173-6915C>G
NM_001370074.1:c.173-6915C>G	NP_001357003.1:n.173-6915C>G
NM_005465.7:c.173-6915C>G MANE Select	NP_005456.1:n.173-6915C>G
NM_001206729.2:c.173-6915C>G	NP_001193658.1:n.173-6915C>G