Canonical Allele Identifier: CA41022931

Gene: AKT3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243545520T>C , CM000663.2:g.243545520T>C	GRCh38
NC_000001.10:g.243708822T>C , CM000663.1:g.243708822T>C	GRCh37
NC_000001.9:g.241775445T>C	NCBI36
NG_029764.1:g.303065A>G
NG_029764.2:g.310560A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005465.7:c.1241A>G MANE Select	NP_005456.1:p.Tyr414Cys
ENST00000673466.1:c.1241A>G MANE Select	ENSP00000500582.1:p.Tyr414Cys
NM_001206729.1:c.1241A>G	NP_001193658.1:p.Tyr414Cys
NM_001206729.2:c.1241A>G	NP_001193658.1:p.Tyr414Cys
NM_001370074.1:c.1241A>G	NP_001357003.1:p.Tyr414Cys
NM_005465.4:c.1241A>G	NP_005456.1:p.Tyr414Cys
NM_005465.5:c.1241A>G	NP_005456.1:p.Tyr414Cys
NM_181690.2:c.1241A>G	NP_859029.1:p.Tyr414Cys
ENST00000263826.12:c.1241A>G	ENSP00000263826.5:p.Tyr414Cys
ENST00000263826.9:c.1241A>G	ENSP00000263826.5:p.Tyr414Cys
ENST00000336199.9:c.1241A>G	ENSP00000336943.5:p.Tyr414Cys
ENST00000366539.5:c.1241A>G	ENSP00000355497.1:p.Tyr414Cys
ENST00000366539.6:c.1172A>G	ENSP00000355497.2:p.Tyr391Cys
ENST00000366540.5:c.1241A>G	ENSP00000355498.1:p.Tyr414Cys
ENST00000672460.1:c.998A>G	ENSP00000499842.1:p.Tyr333Cys
ENST00000672578.1:c.1058A>G	ENSP00000500597.1:p.Tyr353Cys
ENST00000679831.1:n.2252A>G
ENST00000680056.1:c.1115A>G	ENSP00000505337.1:p.Tyr372Cys
ENST00000680118.1:c.1241A>G	ENSP00000505276.1:p.Tyr414Cys
ENST00000681055.1:n.129A>G
ENST00000681794.1:c.1344A>G	ENSP00000506399.1:n.1344A>G
XM_005272994.3:c.1241A>G	XP_005273051.1:p.Tyr414Cys
XM_005272995.2:c.1241A>G	XP_005273052.1:p.Tyr414Cys
XM_005272997.3:c.1058A>G	XP_005273054.1:p.Tyr353Cys
XM_011544011.1:c.1115A>G	XP_011542313.1:p.Tyr372Cys
XM_011544012.1:c.1241A>G	XP_011542314.1:p.Tyr414Cys
XM_011544014.1:c.551A>G	XP_011542316.1:p.Tyr184Cys
XM_011544014.2:c.551A>G	XP_011542316.1:p.Tyr184Cys
XM_016999985.1:c.1058A>G	XP_016855474.1:p.Tyr353Cys
XM_024446000.1:c.1241A>G	XP_024301768.1:p.Tyr414Cys