Canonical Allele Identifier: CA41016492

Gene: SDCCAG8 AKT3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243489086G>A , CM000663.2:g.243489086G>A	GRCh38
NC_000001.10:g.243652388G>A , CM000663.1:g.243652388G>A	GRCh37
NC_000001.9:g.241719011G>A	NCBI36
NG_027811.1:g.238082G>A
NG_029764.1:g.359499C>T
NG_029764.2:g.366994C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006642.5:c.2058G>A (SDCCAG8) MANE Select	NP_006633.1:p.Gln686=
ENST00000366541.8:c.2058G>A (SDCCAG8) MANE Select	ENSP00000355499.3:p.Gln686=
NM_001350246.1:c.1155G>A (SDCCAG8)	NP_001337175.1:p.Gln385=
NM_001350246.2:c.1155G>A (SDCCAG8)	NP_001337175.1:p.Gln385=
NM_001350247.1:c.1155G>A (SDCCAG8)	NP_001337176.1:p.Gln385=
NM_001350247.2:c.1155G>A (SDCCAG8)	NP_001337176.1:p.Gln385=
NM_001350248.1:c.2154G>A (SDCCAG8)	NP_001337177.1:p.Gln718=
NM_001350248.2:c.2154G>A (SDCCAG8)	NP_001337177.1:p.Gln718=
NM_001350249.1:c.1764G>A (SDCCAG8)	NP_001337178.1:p.Gln588=
NM_001350249.2:c.1764G>A (SDCCAG8)	NP_001337178.1:p.Gln588=
NM_001350251.1:c.1155G>A (SDCCAG8)	NP_001337180.1:p.Gln385=
NM_001350251.2:c.1155G>A (SDCCAG8)	NP_001337180.1:p.Gln385=
NM_006642.3:c.2058G>A (SDCCAG8)	NP_006633.1:p.Gln686=
NM_006642.4:c.2058G>A (SDCCAG8)	NP_006633.1:p.Gln686=
NM_181690.2:c.*7-636C>T (AKT3)	NP_859029.1:n.*7-636C>T
ENST00000336199.9:c.*7-636C>T (AKT3)	ENSP00000336943.5:n.*7-636C>T
ENST00000366541.7:c.2058G>A (SDCCAG8)	ENSP00000355499.3:p.Gln686=
ENST00000435549.1:c.1161G>A (SDCCAG8)	ENSP00000410200.1:p.Gln387=
ENST00000497459.1:n.137G>A (SDCCAG8)
XM_005273013.3:c.1929G>A (SDCCAG8)	XP_005273070.1:p.Gln643=
XM_005273013.5:c.1929G>A (SDCCAG8)	XP_005273070.1:p.Gln643=
XM_005273018.1:c.1635G>A (SDCCAG8)	XP_005273075.1:p.Gln545=
XM_005273018.2:c.1635G>A (SDCCAG8)	XP_005273075.1:p.Gln545=
XM_005273021.3:c.1155G>A (SDCCAG8)	XP_005273078.1:p.Gln385=
XM_005273022.2:c.1137G>A (SDCCAG8)	XP_005273079.1:p.Gln379=
XM_005273022.4:c.1137G>A (SDCCAG8)	XP_005273079.1:p.Gln379=
XM_006711727.2:c.2088G>A (SDCCAG8)	XP_006711790.1:p.Gln696=
XM_006711728.2:c.1959G>A (SDCCAG8)	XP_006711791.1:p.Gln653=
XM_006711729.2:c.1899G>A (SDCCAG8)	XP_006711792.1:p.Gln633=
XM_011544021.1:c.2184G>A (SDCCAG8)	XP_011542323.1:p.Gln728=
XM_011544022.1:c.2154G>A (SDCCAG8)	XP_011542324.1:p.Gln718=
XM_011544024.1:c.2112-10670G>A (SDCCAG8)	XP_011542326.1:n.2112-10670G>A
XM_011544025.1:c.1995G>A (SDCCAG8)	XP_011542327.1:p.Gln665=
XM_011544026.1:c.1947G>A (SDCCAG8)	XP_011542328.1:p.Gln649=
XM_011544026.3:c.1947G>A (SDCCAG8)	XP_011542328.1:p.Gln649=
XM_011544027.1:c.1770G>A (SDCCAG8)	XP_011542329.1:p.Gln590=
XM_011544028.1:c.1722G>A (SDCCAG8)	XP_011542330.1:p.Gln574=
XM_011544028.3:c.1722G>A (SDCCAG8)	XP_011542330.1:p.Gln574=
XM_011544030.1:c.1113G>A (SDCCAG8)	XP_011542332.1:p.Gln371=
XM_011544030.3:c.1113G>A (SDCCAG8)	XP_011542332.1:p.Gln371=
XM_017000105.2:c.1821G>A (SDCCAG8)	XP_016855594.1:p.Gln607=
XM_024452537.1:c.1860G>A (SDCCAG8)	XP_024308305.1:p.Gln620=
XM_024452540.1:c.1860G>A (SDCCAG8)	XP_024308308.1:p.Gln620=
XM_024452548.1:c.1860G>A (SDCCAG8)	XP_024308316.1:p.Gln620=
XM_024452549.1:c.1527G>A (SDCCAG8)	XP_024308317.1:p.Gln509=
XR_002958955.1:n.2100G>A (SDCCAG8)
XR_002958965.1:n.1991G>A (SDCCAG8)