Canonical Allele Identifier: CA1230390618

Gene: SDCCAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426529T= , CM000663.2:g.243426529T=	GRCh38
NC_000001.10:g.243589831T= , CM000663.1:g.243589831T=	GRCh37
NC_000001.9:g.241656454T=	NCBI36
NG_027811.1:g.175525T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1956T= MANE Select	ENSP00000355499.3:p.His652=
ENST00000366541.7:c.1956T=	ENSP00000355499.3:p.His652=
ENST00000435549.1:c.1059T=	ENSP00000410200.1:p.His353=
ENST00000463042.1:n.163T=
NM_006642.3:c.1956T=	NP_006633.1:p.His652=
XM_005273013.3:c.1827T=	XP_005273070.1:p.His609=
XM_005273018.1:c.1533T=	XP_005273075.1:p.His511=
XM_005273021.3:c.1053T=	XP_005273078.1:p.His351=
XM_005273022.2:c.1035T=	XP_005273079.1:p.His345=
XM_006711727.2:c.1986T=	XP_006711790.1:p.His662=
XM_006711728.2:c.1857T=	XP_006711791.1:p.His619=
XM_006711729.2:c.1797T=	XP_006711792.1:p.His599=
XM_011544021.1:c.2082T=	XP_011542323.1:p.His694=
XM_011544022.1:c.2052T=	XP_011542324.1:p.His684=
XM_011544023.1:c.2082T=	XP_011542325.1:p.His694=
XM_011544024.1:c.2082T=	XP_011542326.1:p.His694=
XM_011544025.1:c.1893T=	XP_011542327.1:p.His631=
XM_011544026.1:c.1845T=	XP_011542328.1:p.His615=
XM_011544027.1:c.1668T=	XP_011542329.1:p.His556=
XM_011544028.1:c.1620T=	XP_011542330.1:p.His540=
XM_011544030.1:c.1011T=	XP_011542332.1:p.His337=
XR_949128.1:n.2106T=
NM_001350246.1:c.1053T=	NP_001337175.1:p.His351=
NM_001350247.1:c.1053T=	NP_001337176.1:p.His351=
NM_001350248.1:c.2052T=	NP_001337177.1:p.His684=
NM_001350249.1:c.1662T=	NP_001337178.1:p.His554=
NM_001350251.1:c.1053T=	NP_001337180.1:p.His351=
NM_006642.4:c.1956T=	NP_006633.1:p.His652=
XM_005273013.5:c.1827T=	XP_005273070.1:p.His609=
XM_005273018.2:c.1533T=	XP_005273075.1:p.His511=
XM_005273022.4:c.1035T=	XP_005273079.1:p.His345=
XM_011544026.3:c.1845T=	XP_011542328.1:p.His615=
XM_011544028.3:c.1620T=	XP_011542330.1:p.His540=
XM_011544030.3:c.1011T=	XP_011542332.1:p.His337=
XM_017000104.2:c.1827T=	XP_016855593.1:p.His609=
XM_017000105.2:c.1719T=	XP_016855594.1:p.His573=
XM_024452537.1:c.1758T=	XP_024308305.1:p.His586=
XM_024452539.1:c.1758T=	XP_024308307.1:p.His586=
XM_024452540.1:c.1758T=	XP_024308308.1:p.His586=
XM_024452547.1:c.1662T=	XP_024308315.1:p.His554=
XM_024452548.1:c.1758T=	XP_024308316.1:p.His586=
XM_024452549.1:c.1425T=	XP_024308317.1:p.His475=
XR_002958955.1:n.1998T=
XR_002958956.1:n.1998T=
XR_002958965.1:n.1889T=
NM_006642.5:c.1956T= MANE Select	NP_006633.1:p.His652=
NM_001350246.2:c.1053T=	NP_001337175.1:p.His351=
NM_001350247.2:c.1053T=	NP_001337176.1:p.His351=
NM_001350248.2:c.2052T=	NP_001337177.1:p.His684=
NM_001350249.2:c.1662T=	NP_001337178.1:p.His554=
NM_001350251.2:c.1053T=	NP_001337180.1:p.His351=