Canonical Allele Identifier: CA41016496
Community Standard Title: NM_006642.5(SDCCAG8):c.2091G>T (p.Glu697Asp)
Gene: SDCCAG8 HGNC NCBI
AKT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.243489119G>T , CM000663.2:g.243489119G>T GRCh38
NC_000001.10:g.243652421G>T , CM000663.1:g.243652421G>T GRCh37
NC_000001.9:g.241719044G>T NCBI36
NG_027811.1:g.238115G>T
NG_029764.1:g.359466C>A
NG_029764.2:g.366961C>A

Transcript Alleles

HGVS Amino-acid Change
NM_006642.5:c.2091G>T (SDCCAG8) MANE Select NP_006633.1:p.Glu697Asp
ENST00000366541.8:c.2091G>T (SDCCAG8) MANE Select ENSP00000355499.3:p.Glu697Asp
NM_001350246.1:c.1188G>T (SDCCAG8) NP_001337175.1:p.Glu396Asp
NM_001350246.2:c.1188G>T (SDCCAG8) NP_001337175.1:p.Glu396Asp
NM_001350247.1:c.1188G>T (SDCCAG8) NP_001337176.1:p.Glu396Asp
NM_001350247.2:c.1188G>T (SDCCAG8) NP_001337176.1:p.Glu396Asp
NM_001350248.1:c.2187G>T (SDCCAG8) NP_001337177.1:p.Glu729Asp
NM_001350248.2:c.2187G>T (SDCCAG8) NP_001337177.1:p.Glu729Asp
NM_001350249.1:c.1797G>T (SDCCAG8) NP_001337178.1:p.Glu599Asp
NM_001350249.2:c.1797G>T (SDCCAG8) NP_001337178.1:p.Glu599Asp
NM_001350251.1:c.1188G>T (SDCCAG8) NP_001337180.1:p.Glu396Asp
NM_001350251.2:c.1188G>T (SDCCAG8) NP_001337180.1:p.Glu396Asp
NM_006642.3:c.2091G>T (SDCCAG8) NP_006633.1:p.Glu697Asp
NM_006642.4:c.2091G>T (SDCCAG8) NP_006633.1:p.Glu697Asp
NM_181690.2:c.*7-669C>A (AKT3) NP_859029.1:n.*7-669C>A
ENST00000336199.9:c.*7-669C>A (AKT3) ENSP00000336943.5:n.*7-669C>A
ENST00000366541.7:c.2091G>T (SDCCAG8) ENSP00000355499.3:p.Glu697Asp
ENST00000435549.1:c.1194G>T (SDCCAG8) ENSP00000410200.1:p.Glu398Asp
ENST00000497459.1:n.170G>T (SDCCAG8)
XM_005273013.3:c.1962G>T (SDCCAG8) XP_005273070.1:p.Glu654Asp
XM_005273013.5:c.1962G>T (SDCCAG8) XP_005273070.1:p.Glu654Asp
XM_005273018.1:c.1668G>T (SDCCAG8) XP_005273075.1:p.Glu556Asp
XM_005273018.2:c.1668G>T (SDCCAG8) XP_005273075.1:p.Glu556Asp
XM_005273021.3:c.1188G>T (SDCCAG8) XP_005273078.1:p.Glu396Asp
XM_005273022.2:c.1170G>T (SDCCAG8) XP_005273079.1:p.Glu390Asp
XM_005273022.4:c.1170G>T (SDCCAG8) XP_005273079.1:p.Glu390Asp
XM_006711727.2:c.2121G>T (SDCCAG8) XP_006711790.1:p.Glu707Asp
XM_006711728.2:c.1992G>T (SDCCAG8) XP_006711791.1:p.Glu664Asp
XM_006711729.2:c.1932G>T (SDCCAG8) XP_006711792.1:p.Glu644Asp
XM_011544021.1:c.2217G>T (SDCCAG8) XP_011542323.1:p.Glu739Asp
XM_011544022.1:c.2187G>T (SDCCAG8) XP_011542324.1:p.Glu729Asp
XM_011544024.1:c.2112-10637G>T (SDCCAG8) XP_011542326.1:n.2112-10637G>T
XM_011544025.1:c.2028G>T (SDCCAG8) XP_011542327.1:p.Glu676Asp
XM_011544026.1:c.1980G>T (SDCCAG8) XP_011542328.1:p.Glu660Asp
XM_011544026.3:c.1980G>T (SDCCAG8) XP_011542328.1:p.Glu660Asp
XM_011544027.1:c.1803G>T (SDCCAG8) XP_011542329.1:p.Glu601Asp
XM_011544028.1:c.1755G>T (SDCCAG8) XP_011542330.1:p.Glu585Asp
XM_011544028.3:c.1755G>T (SDCCAG8) XP_011542330.1:p.Glu585Asp
XM_011544030.1:c.1146G>T (SDCCAG8) XP_011542332.1:p.Glu382Asp
XM_011544030.3:c.1146G>T (SDCCAG8) XP_011542332.1:p.Glu382Asp
XM_017000105.2:c.1854G>T (SDCCAG8) XP_016855594.1:p.Glu618Asp
XM_024452537.1:c.1893G>T (SDCCAG8) XP_024308305.1:p.Glu631Asp
XM_024452540.1:c.1893G>T (SDCCAG8) XP_024308308.1:p.Glu631Asp
XM_024452548.1:c.1893G>T (SDCCAG8) XP_024308316.1:p.Glu631Asp
XM_024452549.1:c.1560G>T (SDCCAG8) XP_024308317.1:p.Glu520Asp
XR_002958955.1:n.2133G>T (SDCCAG8)
XR_002958965.1:n.2024G>T (SDCCAG8)