Canonical Allele Identifier: CA424348537

Gene: SDCCAG8 AKT3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243489056G>A , CM000663.2:g.243489056G>A	GRCh38
NC_000001.10:g.243652358G>A , CM000663.1:g.243652358G>A	GRCh37
NC_000001.9:g.241718981G>A	NCBI36
NG_027811.1:g.238052G>A
NG_029764.1:g.359529C>T
NG_029764.2:g.367024C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006642.5:c.2028G>A (SDCCAG8) MANE Select	NP_006633.1:p.Gln676=
ENST00000366541.8:c.2028G>A (SDCCAG8) MANE Select	ENSP00000355499.3:p.Gln676=
NM_001350246.1:c.1125G>A (SDCCAG8)	NP_001337175.1:p.Gln375=
NM_001350246.2:c.1125G>A (SDCCAG8)	NP_001337175.1:p.Gln375=
NM_001350247.1:c.1125G>A (SDCCAG8)	NP_001337176.1:p.Gln375=
NM_001350247.2:c.1125G>A (SDCCAG8)	NP_001337176.1:p.Gln375=
NM_001350248.1:c.2124G>A (SDCCAG8)	NP_001337177.1:p.Gln708=
NM_001350248.2:c.2124G>A (SDCCAG8)	NP_001337177.1:p.Gln708=
NM_001350249.1:c.1734G>A (SDCCAG8)	NP_001337178.1:p.Gln578=
NM_001350249.2:c.1734G>A (SDCCAG8)	NP_001337178.1:p.Gln578=
NM_001350251.1:c.1125G>A (SDCCAG8)	NP_001337180.1:p.Gln375=
NM_001350251.2:c.1125G>A (SDCCAG8)	NP_001337180.1:p.Gln375=
NM_006642.3:c.2028G>A (SDCCAG8)	NP_006633.1:p.Gln676=
NM_006642.4:c.2028G>A (SDCCAG8)	NP_006633.1:p.Gln676=
NM_181690.2:c.*7-606C>T (AKT3)	NP_859029.1:n.*7-606C>T
ENST00000336199.9:c.*7-606C>T (AKT3)	ENSP00000336943.5:n.*7-606C>T
ENST00000366541.7:c.2028G>A (SDCCAG8)	ENSP00000355499.3:p.Gln676=
ENST00000435549.1:c.1131G>A (SDCCAG8)	ENSP00000410200.1:p.Gln377=
ENST00000497459.1:n.107G>A (SDCCAG8)
XM_005273013.3:c.1899G>A (SDCCAG8)	XP_005273070.1:p.Gln633=
XM_005273013.5:c.1899G>A (SDCCAG8)	XP_005273070.1:p.Gln633=
XM_005273018.1:c.1605G>A (SDCCAG8)	XP_005273075.1:p.Gln535=
XM_005273018.2:c.1605G>A (SDCCAG8)	XP_005273075.1:p.Gln535=
XM_005273021.3:c.1125G>A (SDCCAG8)	XP_005273078.1:p.Gln375=
XM_005273022.2:c.1107G>A (SDCCAG8)	XP_005273079.1:p.Gln369=
XM_005273022.4:c.1107G>A (SDCCAG8)	XP_005273079.1:p.Gln369=
XM_006711727.2:c.2058G>A (SDCCAG8)	XP_006711790.1:p.Gln686=
XM_006711728.2:c.1929G>A (SDCCAG8)	XP_006711791.1:p.Gln643=
XM_006711729.2:c.1869G>A (SDCCAG8)	XP_006711792.1:p.Gln623=
XM_011544021.1:c.2154G>A (SDCCAG8)	XP_011542323.1:p.Gln718=
XM_011544022.1:c.2124G>A (SDCCAG8)	XP_011542324.1:p.Gln708=
XM_011544024.1:c.2112-10700G>A (SDCCAG8)	XP_011542326.1:n.2112-10700G>A
XM_011544025.1:c.1965G>A (SDCCAG8)	XP_011542327.1:p.Gln655=
XM_011544026.1:c.1917G>A (SDCCAG8)	XP_011542328.1:p.Gln639=
XM_011544026.3:c.1917G>A (SDCCAG8)	XP_011542328.1:p.Gln639=
XM_011544027.1:c.1740G>A (SDCCAG8)	XP_011542329.1:p.Gln580=
XM_011544028.1:c.1692G>A (SDCCAG8)	XP_011542330.1:p.Gln564=
XM_011544028.3:c.1692G>A (SDCCAG8)	XP_011542330.1:p.Gln564=
XM_011544030.1:c.1083G>A (SDCCAG8)	XP_011542332.1:p.Gln361=
XM_011544030.3:c.1083G>A (SDCCAG8)	XP_011542332.1:p.Gln361=
XM_017000105.2:c.1791G>A (SDCCAG8)	XP_016855594.1:p.Gln597=
XM_024452537.1:c.1830G>A (SDCCAG8)	XP_024308305.1:p.Gln610=
XM_024452540.1:c.1830G>A (SDCCAG8)	XP_024308308.1:p.Gln610=
XM_024452548.1:c.1830G>A (SDCCAG8)	XP_024308316.1:p.Gln610=
XM_024452549.1:c.1497G>A (SDCCAG8)	XP_024308317.1:p.Gln499=
XR_002958955.1:n.2070G>A (SDCCAG8)
XR_002958965.1:n.1961G>A (SDCCAG8)