Canonical Allele Identifier: CA424348579

Gene: SDCCAG8 AKT3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243489128G>C , CM000663.2:g.243489128G>C	GRCh38
NC_000001.10:g.243652430G>C , CM000663.1:g.243652430G>C	GRCh37
NC_000001.9:g.241719053G>C	NCBI36
NG_027811.1:g.238124G>C
NG_029764.1:g.359457C>G
NG_029764.2:g.366952C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006642.5:c.2100G>C (SDCCAG8) MANE Select	NP_006633.1:p.Arg700=
ENST00000366541.8:c.2100G>C (SDCCAG8) MANE Select	ENSP00000355499.3:p.Arg700=
NM_001350246.1:c.1197G>C (SDCCAG8)	NP_001337175.1:p.Arg399=
NM_001350246.2:c.1197G>C (SDCCAG8)	NP_001337175.1:p.Arg399=
NM_001350247.1:c.1197G>C (SDCCAG8)	NP_001337176.1:p.Arg399=
NM_001350247.2:c.1197G>C (SDCCAG8)	NP_001337176.1:p.Arg399=
NM_001350248.1:c.2196G>C (SDCCAG8)	NP_001337177.1:p.Arg732=
NM_001350248.2:c.2196G>C (SDCCAG8)	NP_001337177.1:p.Arg732=
NM_001350249.1:c.1806G>C (SDCCAG8)	NP_001337178.1:p.Arg602=
NM_001350249.2:c.1806G>C (SDCCAG8)	NP_001337178.1:p.Arg602=
NM_001350251.1:c.1197G>C (SDCCAG8)	NP_001337180.1:p.Arg399=
NM_001350251.2:c.1197G>C (SDCCAG8)	NP_001337180.1:p.Arg399=
NM_006642.3:c.2100G>C (SDCCAG8)	NP_006633.1:p.Arg700=
NM_006642.4:c.2100G>C (SDCCAG8)	NP_006633.1:p.Arg700=
NM_181690.2:c.*7-678C>G (AKT3)	NP_859029.1:n.*7-678C>G
ENST00000336199.9:c.*7-678C>G (AKT3)	ENSP00000336943.5:n.*7-678C>G
ENST00000366541.7:c.2100G>C (SDCCAG8)	ENSP00000355499.3:p.Arg700=
ENST00000435549.1:c.1203G>C (SDCCAG8)	ENSP00000410200.1:p.Arg401=
ENST00000497459.1:n.179G>C (SDCCAG8)
XM_005273013.3:c.1971G>C (SDCCAG8)	XP_005273070.1:p.Arg657=
XM_005273013.5:c.1971G>C (SDCCAG8)	XP_005273070.1:p.Arg657=
XM_005273018.1:c.1677G>C (SDCCAG8)	XP_005273075.1:p.Arg559=
XM_005273018.2:c.1677G>C (SDCCAG8)	XP_005273075.1:p.Arg559=
XM_005273021.3:c.1197G>C (SDCCAG8)	XP_005273078.1:p.Arg399=
XM_005273022.2:c.1179G>C (SDCCAG8)	XP_005273079.1:p.Arg393=
XM_005273022.4:c.1179G>C (SDCCAG8)	XP_005273079.1:p.Arg393=
XM_006711727.2:c.2130G>C (SDCCAG8)	XP_006711790.1:p.Arg710=
XM_006711728.2:c.2001G>C (SDCCAG8)	XP_006711791.1:p.Arg667=
XM_006711729.2:c.1941G>C (SDCCAG8)	XP_006711792.1:p.Arg647=
XM_011544021.1:c.2226G>C (SDCCAG8)	XP_011542323.1:p.Arg742=
XM_011544022.1:c.2196G>C (SDCCAG8)	XP_011542324.1:p.Arg732=
XM_011544024.1:c.2112-10628G>C (SDCCAG8)	XP_011542326.1:n.2112-10628G>C
XM_011544025.1:c.2037G>C (SDCCAG8)	XP_011542327.1:p.Arg679=
XM_011544026.1:c.1989G>C (SDCCAG8)	XP_011542328.1:p.Arg663=
XM_011544026.3:c.1989G>C (SDCCAG8)	XP_011542328.1:p.Arg663=
XM_011544027.1:c.1812G>C (SDCCAG8)	XP_011542329.1:p.Arg604=
XM_011544028.1:c.1764G>C (SDCCAG8)	XP_011542330.1:p.Arg588=
XM_011544028.3:c.1764G>C (SDCCAG8)	XP_011542330.1:p.Arg588=
XM_011544030.1:c.1155G>C (SDCCAG8)	XP_011542332.1:p.Arg385=
XM_011544030.3:c.1155G>C (SDCCAG8)	XP_011542332.1:p.Arg385=
XM_017000105.2:c.1863G>C (SDCCAG8)	XP_016855594.1:p.Arg621=
XM_024452537.1:c.1902G>C (SDCCAG8)	XP_024308305.1:p.Arg634=
XM_024452540.1:c.1902G>C (SDCCAG8)	XP_024308308.1:p.Arg634=
XM_024452548.1:c.1902G>C (SDCCAG8)	XP_024308316.1:p.Arg634=
XM_024452549.1:c.1569G>C (SDCCAG8)	XP_024308317.1:p.Arg523=
XR_002958955.1:n.2142G>C (SDCCAG8)
XR_002958965.1:n.2033G>C (SDCCAG8)