Canonical Allele Identifier: CA2581721533

Gene: AKT3 SDCCAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243500591C>G , CM000663.2:g.243500591C>G	GRCh38
NC_000001.10:g.243663893C>G , CM000663.1:g.243663893C>G	GRCh37
NC_000001.9:g.241730516C>G	NCBI36
NG_027811.1:g.249587C>G
NG_029764.1:g.347994G>C
NG_029764.2:g.355489G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005465.7:c.*4658G>C (AKT3) MANE Select	NP_005456.1:n.*4658G>C
ENST00000673466.1:c.*4658G>C (AKT3) MANE Select	ENSP00000500582.1:n.*4658G>C
NM_001206729.1:c.1355-805G>C (AKT3)	NP_001193658.1:n.1355-805G>C
NM_001206729.2:c.1355-805G>C (AKT3)	NP_001193658.1:n.1355-805G>C
NM_001370074.1:c.*4658G>C (AKT3)	NP_001357003.1:n.*4658G>C
NM_005465.4:c.*4658G>C (AKT3)	NP_005456.1:n.*4658G>C
NM_005465.5:c.*4658G>C (AKT3)	NP_005456.1:n.*4658G>C
NM_181690.2:c.1355-805G>C (AKT3)	NP_859029.1:n.1355-805G>C
ENST00000263826.9:c.*4658G>C (AKT3)	ENSP00000263826.5:n.*4658G>C
ENST00000336199.9:c.1355-805G>C (AKT3)	ENSP00000336943.5:n.1355-805G>C
ENST00000366540.5:c.1355-805G>C (AKT3)	ENSP00000355498.1:n.1355-805G>C
ENST00000672460.1:c.2059-805G>C (AKT3)	ENSP00000499842.1:n.2059-805G>C
ENST00000679831.1:n.7109G>C (AKT3)
ENST00000680118.1:c.*902-805G>C (AKT3)	ENSP00000505276.1:n.*902-805G>C
ENST00000681055.1:n.4986G>C (AKT3)
XM_005272994.3:c.*4658G>C (AKT3)	XP_005273051.1:n.*4658G>C
XM_005272995.2:c.*4658G>C (AKT3)	XP_005273052.1:n.*4658G>C
XM_005272997.3:c.*4658G>C (AKT3)	XP_005273054.1:n.*4658G>C
XM_005273013.5:c.*806C>G (SDCCAG8)	XP_005273070.1:n.*806C>G
XM_005273022.4:c.*806C>G (SDCCAG8)	XP_005273079.1:n.*806C>G
XM_011544011.1:c.*4658G>C (AKT3)	XP_011542313.1:n.*4658G>C
XM_011544014.1:c.*4658G>C (AKT3)	XP_011542316.1:n.*4658G>C
XM_011544030.3:c.*806C>G (SDCCAG8)	XP_011542332.1:n.*806C>G
XM_017000105.2:c.*806C>G (SDCCAG8)	XP_016855594.1:n.*806C>G
XM_024452537.1:c.*2719C>G (SDCCAG8)	XP_024308305.1:n.*2719C>G
XM_024452548.1:c.*806C>G (SDCCAG8)	XP_024308316.1:n.*806C>G
XR_002958955.1:n.3083C>G (SDCCAG8)