Canonical Allele Identifier: CA1014173567
Gene: AKT3 HGNC NCBI

Linked Data

dbSNP Id: rs1683193133

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.243672105_243672106del , CM000663.2:g.243672105_243672106del GRCh38
NC_000001.10:g.243835407_243835408del , CM000663.1:g.243835407_243835408del GRCh37
NC_000001.9:g.241902030_241902031del NCBI36
NG_029764.1:g.176482_176483del
NG_029764.2:g.183977_183978del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263826.12:c.173-7220_173-7219del ENSP00000263826.5:n.173-7220_173-7219del
ENST00000366539.6:c.173-7220_173-7219del ENSP00000355497.2:n.173-7220_173-7219del
ENST00000492957.2:c.173-7220_173-7219del ENSP00000506695.1:n.173-7220_173-7219del
ENST00000552631.2:n.287-7220_287-7219del
ENST00000672238.1:c.173-7220_173-7219del ENSP00000506535.1:n.173-7220_173-7219del
ENST00000672442.1:c.*2-7220_*2-7219del ENSP00000500134.1:n.*2-7220_*2-7219del
ENST00000672578.1:c.-11-7220_-11-7219del ENSP00000500597.1:n.-11-7220_-11-7219del
ENST00000672679.1:n.130-7220_130-7219del
ENST00000673466.1:c.173-7220_173-7219del MANE Select ENSP00000500582.1:n.173-7220_173-7219del
ENST00000680056.1:c.47-7220_47-7219del ENSP00000505337.1:n.47-7220_47-7219del
ENST00000680118.1:c.173-7220_173-7219del ENSP00000505276.1:n.173-7220_173-7219del
ENST00000681794.1:c.173-7220_173-7219del ENSP00000506399.1:n.173-7220_173-7219del
ENST00000263826.9:c.173-7220_173-7219del ENSP00000263826.5:n.173-7220_173-7219del
ENST00000336199.9:c.173-7220_173-7219del ENSP00000336943.5:n.173-7220_173-7219del
ENST00000366539.5:c.173-7220_173-7219del ENSP00000355497.1:n.173-7220_173-7219del
ENST00000366540.5:c.173-7220_173-7219del ENSP00000355498.1:n.173-7220_173-7219del
ENST00000463991.5:n.311-7220_311-7219del
ENST00000552631.1:c.173-7220_173-7219del ENSP00000447820.1:n.173-7220_173-7219del
NM_001206729.1:c.173-7220_173-7219del NP_001193658.1:n.173-7220_173-7219del
NM_005465.4:c.173-7220_173-7219del NP_005456.1:n.173-7220_173-7219del
NM_181690.2:c.173-7220_173-7219del NP_859029.1:n.173-7220_173-7219del
XM_005272994.3:c.173-7220_173-7219del XP_005273051.1:n.173-7220_173-7219del
XM_005272995.2:c.173-7220_173-7219del XP_005273052.1:n.173-7220_173-7219del
XM_005272997.3:c.-11-7220_-11-7219del XP_005273054.1:n.-11-7220_-11-7219del
XM_006711726.2:c.173-7220_173-7219del XP_006711789.1:n.173-7220_173-7219del
XM_011544011.1:c.47-7220_47-7219del XP_011542313.1:n.47-7220_47-7219del
XM_011544012.1:c.173-7220_173-7219del XP_011542314.1:n.173-7220_173-7219del
XM_011544013.1:c.173-7220_173-7219del XP_011542315.1:n.173-7220_173-7219del
XM_016999985.1:c.-11-7220_-11-7219del XP_016855474.1:n.-11-7220_-11-7219del
XM_024446000.1:c.173-7220_173-7219del XP_024301768.1:n.173-7220_173-7219del
XM_024446892.1:c.173-7220_173-7219del XP_024302660.1:n.173-7220_173-7219del
XM_024447938.1:c.173-7220_173-7219del XP_024303706.1:n.173-7220_173-7219del
NM_005465.5:c.173-7220_173-7219del NP_005456.1:n.173-7220_173-7219del
NM_001370074.1:c.173-7220_173-7219del NP_001357003.1:n.173-7220_173-7219del
NM_005465.7:c.173-7220_173-7219del MANE Select NP_005456.1:n.173-7220_173-7219del
NM_001206729.2:c.173-7220_173-7219del NP_001193658.1:n.173-7220_173-7219del