Canonical Allele Identifier: CA1230390586

Gene: SDCCAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426427A= , CM000663.2:g.243426427A=	GRCh38
NC_000001.10:g.243589729A= , CM000663.1:g.243589729A=	GRCh37
NC_000001.9:g.241656352A=	NCBI36
NG_027811.1:g.175423A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1854A= MANE Select	ENSP00000355499.3:p.Arg618=
ENST00000366541.7:c.1854A=	ENSP00000355499.3:p.Arg618=
ENST00000435549.1:c.957A=	ENSP00000410200.1:p.Arg319=
ENST00000463042.1:n.61A=
NM_006642.3:c.1854A=	NP_006633.1:p.Arg618=
XM_005273013.3:c.1725A=	XP_005273070.1:p.Arg575=
XM_005273018.1:c.1431A=	XP_005273075.1:p.Arg477=
XM_005273021.3:c.951A=	XP_005273078.1:p.Arg317=
XM_005273022.2:c.933A=	XP_005273079.1:p.Arg311=
XM_006711727.2:c.1884A=	XP_006711790.1:p.Arg628=
XM_006711728.2:c.1755A=	XP_006711791.1:p.Arg585=
XM_006711729.2:c.1695A=	XP_006711792.1:p.Arg565=
XM_011544021.1:c.1980A=	XP_011542323.1:p.Arg660=
XM_011544022.1:c.1950A=	XP_011542324.1:p.Arg650=
XM_011544023.1:c.1980A=	XP_011542325.1:p.Arg660=
XM_011544024.1:c.1980A=	XP_011542326.1:p.Arg660=
XM_011544025.1:c.1791A=	XP_011542327.1:p.Arg597=
XM_011544026.1:c.1743A=	XP_011542328.1:p.Arg581=
XM_011544027.1:c.1566A=	XP_011542329.1:p.Arg522=
XM_011544028.1:c.1518A=	XP_011542330.1:p.Arg506=
XM_011544030.1:c.909A=	XP_011542332.1:p.Arg303=
XR_949128.1:n.2004A=
NM_001350246.1:c.951A=	NP_001337175.1:p.Arg317=
NM_001350247.1:c.951A=	NP_001337176.1:p.Arg317=
NM_001350248.1:c.1950A=	NP_001337177.1:p.Arg650=
NM_001350249.1:c.1560A=	NP_001337178.1:p.Arg520=
NM_001350251.1:c.951A=	NP_001337180.1:p.Arg317=
NM_006642.4:c.1854A=	NP_006633.1:p.Arg618=
XM_005273013.5:c.1725A=	XP_005273070.1:p.Arg575=
XM_005273018.2:c.1431A=	XP_005273075.1:p.Arg477=
XM_005273022.4:c.933A=	XP_005273079.1:p.Arg311=
XM_011544026.3:c.1743A=	XP_011542328.1:p.Arg581=
XM_011544028.3:c.1518A=	XP_011542330.1:p.Arg506=
XM_011544030.3:c.909A=	XP_011542332.1:p.Arg303=
XM_017000104.2:c.1725A=	XP_016855593.1:p.Arg575=
XM_017000105.2:c.1617A=	XP_016855594.1:p.Arg539=
XM_024452537.1:c.1656A=	XP_024308305.1:p.Arg552=
XM_024452539.1:c.1656A=	XP_024308307.1:p.Arg552=
XM_024452540.1:c.1656A=	XP_024308308.1:p.Arg552=
XM_024452547.1:c.1560A=	XP_024308315.1:p.Arg520=
XM_024452548.1:c.1656A=	XP_024308316.1:p.Arg552=
XM_024452549.1:c.1323A=	XP_024308317.1:p.Arg441=
XR_002958955.1:n.1896A=
XR_002958956.1:n.1896A=
XR_002958965.1:n.1787A=
NM_006642.5:c.1854A= MANE Select	NP_006633.1:p.Arg618=
NM_001350246.2:c.951A=	NP_001337175.1:p.Arg317=
NM_001350247.2:c.951A=	NP_001337176.1:p.Arg317=
NM_001350248.2:c.1950A=	NP_001337177.1:p.Arg650=
NM_001350249.2:c.1560A=	NP_001337178.1:p.Arg520=
NM_001350251.2:c.951A=	NP_001337180.1:p.Arg317=