Canonical Allele Identifier: CA424105462

Gene: SDCCAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243316839A>G , CM000663.2:g.243316839A>G	GRCh38
NC_000001.10:g.243480141A>G , CM000663.1:g.243480141A>G	GRCh37
NC_000001.9:g.241546764A>G	NCBI36
NG_027811.1:g.65835A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006642.5:c.1014A>G MANE Select	NP_006633.1:p.Glu338=
ENST00000366541.8:c.1014A>G MANE Select	ENSP00000355499.3:p.Glu338=
NM_001350246.1:c.111A>G	NP_001337175.1:p.Glu37=
NM_001350246.2:c.111A>G	NP_001337175.1:p.Glu37=
NM_001350247.1:c.111A>G	NP_001337176.1:p.Glu37=
NM_001350247.2:c.111A>G	NP_001337176.1:p.Glu37=
NM_001350248.1:c.1110A>G	NP_001337177.1:p.Glu370=
NM_001350248.2:c.1110A>G	NP_001337177.1:p.Glu370=
NM_001350249.1:c.720A>G	NP_001337178.1:p.Glu240=
NM_001350249.2:c.720A>G	NP_001337178.1:p.Glu240=
NM_001350251.1:c.111A>G	NP_001337180.1:p.Glu37=
NM_001350251.2:c.111A>G	NP_001337180.1:p.Glu37=
NM_006642.3:c.1014A>G	NP_006633.1:p.Glu338=
NM_006642.4:c.1014A>G	NP_006633.1:p.Glu338=
ENST00000366541.7:c.1014A>G	ENSP00000355499.3:p.Glu338=
ENST00000435549.1:c.354A>G	ENSP00000410200.1:p.Glu118=
ENST00000463012.1:n.374A>G
XM_005273013.3:c.885A>G	XP_005273070.1:p.Glu295=
XM_005273013.5:c.885A>G	XP_005273070.1:p.Glu295=
XM_005273018.1:c.591A>G	XP_005273075.1:p.Glu197=
XM_005273018.2:c.591A>G	XP_005273075.1:p.Glu197=
XM_005273021.3:c.111A>G	XP_005273078.1:p.Glu37=
XM_005273022.2:c.93A>G	XP_005273079.1:p.Glu31=
XM_005273022.4:c.93A>G	XP_005273079.1:p.Glu31=
XM_005273023.3:c.1014A>G	XP_005273080.1:p.Glu338=
XM_005273023.5:c.1014A>G	XP_005273080.1:p.Glu338=
XM_006711727.2:c.1044A>G	XP_006711790.1:p.Glu348=
XM_006711728.2:c.915A>G	XP_006711791.1:p.Glu305=
XM_006711729.2:c.855A>G	XP_006711792.1:p.Glu285=
XM_011544021.1:c.1140A>G	XP_011542323.1:p.Glu380=
XM_011544022.1:c.1110A>G	XP_011542324.1:p.Glu370=
XM_011544023.1:c.1140A>G	XP_011542325.1:p.Glu380=
XM_011544024.1:c.1140A>G	XP_011542326.1:p.Glu380=
XM_011544025.1:c.951A>G	XP_011542327.1:p.Glu317=
XM_011544026.1:c.1140A>G	XP_011542328.1:p.Glu380=
XM_011544026.3:c.1140A>G	XP_011542328.1:p.Glu380=
XM_011544027.1:c.726A>G	XP_011542329.1:p.Glu242=
XM_011544028.1:c.915A>G	XP_011542330.1:p.Glu305=
XM_011544028.3:c.915A>G	XP_011542330.1:p.Glu305=
XM_011544029.1:c.1140A>G	XP_011542331.1:p.Glu380=
XM_011544030.1:c.69A>G	XP_011542332.1:p.Glu23=
XM_011544030.3:c.69A>G	XP_011542332.1:p.Glu23=
XM_017000104.2:c.885A>G	XP_016855593.1:p.Glu295=
XM_017000105.2:c.1014A>G	XP_016855594.1:p.Glu338=
XM_024452537.1:c.816A>G	XP_024308305.1:p.Glu272=
XM_024452539.1:c.816A>G	XP_024308307.1:p.Glu272=
XM_024452540.1:c.816A>G	XP_024308308.1:p.Glu272=
XM_024452547.1:c.720A>G	XP_024308315.1:p.Glu240=
XM_024452548.1:c.816A>G	XP_024308316.1:p.Glu272=
XM_024452549.1:c.720A>G	XP_024308317.1:p.Glu240=
XR_002958955.1:n.1056A>G
XR_002958956.1:n.1056A>G
XR_002958965.1:n.1056A>G
XR_949128.1:n.1164A>G