Canonical Allele Identifier: CA1230390588

Gene: SDCCAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426432A= , CM000663.2:g.243426432A=	GRCh38
NC_000001.10:g.243589734A= , CM000663.1:g.243589734A=	GRCh37
NC_000001.9:g.241656357A=	NCBI36
NG_027811.1:g.175428A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1859A= MANE Select	ENSP00000355499.3:p.Glu620=
ENST00000366541.7:c.1859A=	ENSP00000355499.3:p.Glu620=
ENST00000435549.1:c.962A=	ENSP00000410200.1:p.Glu321=
ENST00000463042.1:n.66A=
NM_006642.3:c.1859A=	NP_006633.1:p.Glu620=
XM_005273013.3:c.1730A=	XP_005273070.1:p.Glu577=
XM_005273018.1:c.1436A=	XP_005273075.1:p.Glu479=
XM_005273021.3:c.956A=	XP_005273078.1:p.Glu319=
XM_005273022.2:c.938A=	XP_005273079.1:p.Glu313=
XM_006711727.2:c.1889A=	XP_006711790.1:p.Glu630=
XM_006711728.2:c.1760A=	XP_006711791.1:p.Glu587=
XM_006711729.2:c.1700A=	XP_006711792.1:p.Glu567=
XM_011544021.1:c.1985A=	XP_011542323.1:p.Glu662=
XM_011544022.1:c.1955A=	XP_011542324.1:p.Glu652=
XM_011544023.1:c.1985A=	XP_011542325.1:p.Glu662=
XM_011544024.1:c.1985A=	XP_011542326.1:p.Glu662=
XM_011544025.1:c.1796A=	XP_011542327.1:p.Glu599=
XM_011544026.1:c.1748A=	XP_011542328.1:p.Glu583=
XM_011544027.1:c.1571A=	XP_011542329.1:p.Glu524=
XM_011544028.1:c.1523A=	XP_011542330.1:p.Glu508=
XM_011544030.1:c.914A=	XP_011542332.1:p.Glu305=
XR_949128.1:n.2009A=
NM_001350246.1:c.956A=	NP_001337175.1:p.Glu319=
NM_001350247.1:c.956A=	NP_001337176.1:p.Glu319=
NM_001350248.1:c.1955A=	NP_001337177.1:p.Glu652=
NM_001350249.1:c.1565A=	NP_001337178.1:p.Glu522=
NM_001350251.1:c.956A=	NP_001337180.1:p.Glu319=
NM_006642.4:c.1859A=	NP_006633.1:p.Glu620=
XM_005273013.5:c.1730A=	XP_005273070.1:p.Glu577=
XM_005273018.2:c.1436A=	XP_005273075.1:p.Glu479=
XM_005273022.4:c.938A=	XP_005273079.1:p.Glu313=
XM_011544026.3:c.1748A=	XP_011542328.1:p.Glu583=
XM_011544028.3:c.1523A=	XP_011542330.1:p.Glu508=
XM_011544030.3:c.914A=	XP_011542332.1:p.Glu305=
XM_017000104.2:c.1730A=	XP_016855593.1:p.Glu577=
XM_017000105.2:c.1622A=	XP_016855594.1:p.Glu541=
XM_024452537.1:c.1661A=	XP_024308305.1:p.Glu554=
XM_024452539.1:c.1661A=	XP_024308307.1:p.Glu554=
XM_024452540.1:c.1661A=	XP_024308308.1:p.Glu554=
XM_024452547.1:c.1565A=	XP_024308315.1:p.Glu522=
XM_024452548.1:c.1661A=	XP_024308316.1:p.Glu554=
XM_024452549.1:c.1328A=	XP_024308317.1:p.Glu443=
XR_002958955.1:n.1901A=
XR_002958956.1:n.1901A=
XR_002958965.1:n.1792A=
NM_006642.5:c.1859A= MANE Select	NP_006633.1:p.Glu620=
NM_001350246.2:c.956A=	NP_001337175.1:p.Glu319=
NM_001350247.2:c.956A=	NP_001337176.1:p.Glu319=
NM_001350248.2:c.1955A=	NP_001337177.1:p.Glu652=
NM_001350249.2:c.1565A=	NP_001337178.1:p.Glu522=
NM_001350251.2:c.956A=	NP_001337180.1:p.Glu319=