Canonical Allele Identifier: CA41016491

Gene: SDCCAG8 AKT3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243489059G>A , CM000663.2:g.243489059G>A	GRCh38
NC_000001.10:g.243652361G>A , CM000663.1:g.243652361G>A	GRCh37
NC_000001.9:g.241718984G>A	NCBI36
NG_027811.1:g.238055G>A
NG_029764.1:g.359526C>T
NG_029764.2:g.367021C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006642.5:c.2031G>A (SDCCAG8) MANE Select	NP_006633.1:p.Leu677=
ENST00000366541.8:c.2031G>A (SDCCAG8) MANE Select	ENSP00000355499.3:p.Leu677=
NM_001350246.1:c.1128G>A (SDCCAG8)	NP_001337175.1:p.Leu376=
NM_001350246.2:c.1128G>A (SDCCAG8)	NP_001337175.1:p.Leu376=
NM_001350247.1:c.1128G>A (SDCCAG8)	NP_001337176.1:p.Leu376=
NM_001350247.2:c.1128G>A (SDCCAG8)	NP_001337176.1:p.Leu376=
NM_001350248.1:c.2127G>A (SDCCAG8)	NP_001337177.1:p.Leu709=
NM_001350248.2:c.2127G>A (SDCCAG8)	NP_001337177.1:p.Leu709=
NM_001350249.1:c.1737G>A (SDCCAG8)	NP_001337178.1:p.Leu579=
NM_001350249.2:c.1737G>A (SDCCAG8)	NP_001337178.1:p.Leu579=
NM_001350251.1:c.1128G>A (SDCCAG8)	NP_001337180.1:p.Leu376=
NM_001350251.2:c.1128G>A (SDCCAG8)	NP_001337180.1:p.Leu376=
NM_006642.3:c.2031G>A (SDCCAG8)	NP_006633.1:p.Leu677=
NM_006642.4:c.2031G>A (SDCCAG8)	NP_006633.1:p.Leu677=
NM_181690.2:c.*7-609C>T (AKT3)	NP_859029.1:n.*7-609C>T
ENST00000336199.9:c.*7-609C>T (AKT3)	ENSP00000336943.5:n.*7-609C>T
ENST00000366541.7:c.2031G>A (SDCCAG8)	ENSP00000355499.3:p.Leu677=
ENST00000435549.1:c.1134G>A (SDCCAG8)	ENSP00000410200.1:p.Leu378=
ENST00000497459.1:n.110G>A (SDCCAG8)
XM_005273013.3:c.1902G>A (SDCCAG8)	XP_005273070.1:p.Leu634=
XM_005273013.5:c.1902G>A (SDCCAG8)	XP_005273070.1:p.Leu634=
XM_005273018.1:c.1608G>A (SDCCAG8)	XP_005273075.1:p.Leu536=
XM_005273018.2:c.1608G>A (SDCCAG8)	XP_005273075.1:p.Leu536=
XM_005273021.3:c.1128G>A (SDCCAG8)	XP_005273078.1:p.Leu376=
XM_005273022.2:c.1110G>A (SDCCAG8)	XP_005273079.1:p.Leu370=
XM_005273022.4:c.1110G>A (SDCCAG8)	XP_005273079.1:p.Leu370=
XM_006711727.2:c.2061G>A (SDCCAG8)	XP_006711790.1:p.Leu687=
XM_006711728.2:c.1932G>A (SDCCAG8)	XP_006711791.1:p.Leu644=
XM_006711729.2:c.1872G>A (SDCCAG8)	XP_006711792.1:p.Leu624=
XM_011544021.1:c.2157G>A (SDCCAG8)	XP_011542323.1:p.Leu719=
XM_011544022.1:c.2127G>A (SDCCAG8)	XP_011542324.1:p.Leu709=
XM_011544024.1:c.2112-10697G>A (SDCCAG8)	XP_011542326.1:n.2112-10697G>A
XM_011544025.1:c.1968G>A (SDCCAG8)	XP_011542327.1:p.Leu656=
XM_011544026.1:c.1920G>A (SDCCAG8)	XP_011542328.1:p.Leu640=
XM_011544026.3:c.1920G>A (SDCCAG8)	XP_011542328.1:p.Leu640=
XM_011544027.1:c.1743G>A (SDCCAG8)	XP_011542329.1:p.Leu581=
XM_011544028.1:c.1695G>A (SDCCAG8)	XP_011542330.1:p.Leu565=
XM_011544028.3:c.1695G>A (SDCCAG8)	XP_011542330.1:p.Leu565=
XM_011544030.1:c.1086G>A (SDCCAG8)	XP_011542332.1:p.Leu362=
XM_011544030.3:c.1086G>A (SDCCAG8)	XP_011542332.1:p.Leu362=
XM_017000105.2:c.1794G>A (SDCCAG8)	XP_016855594.1:p.Leu598=
XM_024452537.1:c.1833G>A (SDCCAG8)	XP_024308305.1:p.Leu611=
XM_024452540.1:c.1833G>A (SDCCAG8)	XP_024308308.1:p.Leu611=
XM_024452548.1:c.1833G>A (SDCCAG8)	XP_024308316.1:p.Leu611=
XM_024452549.1:c.1500G>A (SDCCAG8)	XP_024308317.1:p.Leu500=
XR_002958955.1:n.2073G>A (SDCCAG8)
XR_002958965.1:n.1964G>A (SDCCAG8)