Canonical Allele Identifier: CA913190040

Gene: SDCCAG8

Linked Data

• ClinVar Variation Id: 631599
• ClinVar RCV Id: RCV000778230
• dbSNP Id: rs1558186720

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243256241dup , CM000663.2:g.243256241dup	GRCh38
NC_000001.10:g.243419543dup , CM000663.1:g.243419543dup	GRCh37
NC_000001.9:g.241486166dup	NCBI36
NG_027811.1:g.5237dup
NG_029663.1:g.4169dup
NG_029663.2:g.4169dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.67+1dup
ENST00000366541.7:c.67+1dup
ENST00000490065.5:n.207+1dup
NM_006642.3:c.67+1dup
XM_005273013.3:c.67+1dup
XM_005273018.1:c.-241+1dup
XM_005273022.2:c.-472+1dup
XM_005273023.3:c.67+1dup
XM_006711727.2:c.84+715dup	XP_006711790.1:n.84+715dup
XM_006711728.2:c.84+715dup	XP_006711791.1:n.84+715dup
XM_006711729.2:c.84+715dup	XP_006711792.1:n.84+715dup
XM_011544021.1:c.84+715dup	XP_011542323.1:n.84+715dup
XM_011544022.1:c.67+1dup
XM_011544023.1:c.84+715dup	XP_011542325.1:n.84+715dup
XM_011544024.1:c.84+715dup	XP_011542326.1:n.84+715dup
XM_011544025.1:c.84+715dup	XP_011542327.1:n.84+715dup
XM_011544026.1:c.84+715dup	XP_011542328.1:n.84+715dup
XM_011544027.1:c.84+715dup	XP_011542329.1:n.84+715dup
XM_011544028.1:c.84+715dup	XP_011542330.1:n.84+715dup
XM_011544029.1:c.84+715dup	XP_011542331.1:n.84+715dup
XR_949128.1:n.108+715dup
NM_001350246.1:c.-1046+1dup
NM_001350247.1:c.-934+1dup
NM_001350248.1:c.67+1dup
NM_001350249.1:c.-241+1dup
NM_001350251.1:c.-1307+1dup
NM_006642.4:c.67+1dup
XM_005273013.5:c.67+1dup
XM_005273018.2:c.-241+1dup
XM_005273022.4:c.-472+1dup
XM_005273023.5:c.67+1dup
XM_011544026.3:c.84+715dup	XP_011542328.1:n.84+715dup
XM_011544028.3:c.84+715dup	XP_011542330.1:n.84+715dup
XM_017000104.2:c.67+1dup
XM_017000105.2:c.67+1dup
XM_024452540.1:c.-241+1dup
XM_024452547.1:c.-241+1dup
XM_024452548.1:c.-228+715dup	XP_024308316.1:n.-228+715dup
XM_024452549.1:c.-241+1dup
NM_006642.5:c.67+1dup
NM_001350246.2:c.-1046+1dup
NM_001350247.2:c.-934+1dup
NM_001350248.2:c.67+1dup
NM_001350249.2:c.-241+1dup
NM_001350251.2:c.-1307+1dup