Canonical Allele Identifier: CA424346854

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589756A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426454A>G , CM000663.2:g.243426454A>G	GRCh38
NC_000001.10:g.243589756A>G , CM000663.1:g.243589756A>G	GRCh37
NC_000001.9:g.241656379A>G	NCBI36
NG_027811.1:g.175450A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1881A>G MANE Select	ENSP00000355499.3:p.Glu627=
ENST00000366541.7:c.1881A>G	ENSP00000355499.3:p.Glu627=
ENST00000435549.1:c.984A>G	ENSP00000410200.1:p.Glu328=
ENST00000463042.1:n.88A>G
NM_006642.3:c.1881A>G	NP_006633.1:p.Glu627=
XM_005273013.3:c.1752A>G	XP_005273070.1:p.Glu584=
XM_005273018.1:c.1458A>G	XP_005273075.1:p.Glu486=
XM_005273021.3:c.978A>G	XP_005273078.1:p.Glu326=
XM_005273022.2:c.960A>G	XP_005273079.1:p.Glu320=
XM_006711727.2:c.1911A>G	XP_006711790.1:p.Glu637=
XM_006711728.2:c.1782A>G	XP_006711791.1:p.Glu594=
XM_006711729.2:c.1722A>G	XP_006711792.1:p.Glu574=
XM_011544021.1:c.2007A>G	XP_011542323.1:p.Glu669=
XM_011544022.1:c.1977A>G	XP_011542324.1:p.Glu659=
XM_011544023.1:c.2007A>G	XP_011542325.1:p.Glu669=
XM_011544024.1:c.2007A>G	XP_011542326.1:p.Glu669=
XM_011544025.1:c.1818A>G	XP_011542327.1:p.Glu606=
XM_011544026.1:c.1770A>G	XP_011542328.1:p.Glu590=
XM_011544027.1:c.1593A>G	XP_011542329.1:p.Glu531=
XM_011544028.1:c.1545A>G	XP_011542330.1:p.Glu515=
XM_011544030.1:c.936A>G	XP_011542332.1:p.Glu312=
XR_949128.1:n.2031A>G
NM_001350246.1:c.978A>G	NP_001337175.1:p.Glu326=
NM_001350247.1:c.978A>G	NP_001337176.1:p.Glu326=
NM_001350248.1:c.1977A>G	NP_001337177.1:p.Glu659=
NM_001350249.1:c.1587A>G	NP_001337178.1:p.Glu529=
NM_001350251.1:c.978A>G	NP_001337180.1:p.Glu326=
NM_006642.4:c.1881A>G	NP_006633.1:p.Glu627=
XM_005273013.5:c.1752A>G	XP_005273070.1:p.Glu584=
XM_005273018.2:c.1458A>G	XP_005273075.1:p.Glu486=
XM_005273022.4:c.960A>G	XP_005273079.1:p.Glu320=
XM_011544026.3:c.1770A>G	XP_011542328.1:p.Glu590=
XM_011544028.3:c.1545A>G	XP_011542330.1:p.Glu515=
XM_011544030.3:c.936A>G	XP_011542332.1:p.Glu312=
XM_017000104.2:c.1752A>G	XP_016855593.1:p.Glu584=
XM_017000105.2:c.1644A>G	XP_016855594.1:p.Glu548=
XM_024452537.1:c.1683A>G	XP_024308305.1:p.Glu561=
XM_024452539.1:c.1683A>G	XP_024308307.1:p.Glu561=
XM_024452540.1:c.1683A>G	XP_024308308.1:p.Glu561=
XM_024452547.1:c.1587A>G	XP_024308315.1:p.Glu529=
XM_024452548.1:c.1683A>G	XP_024308316.1:p.Glu561=
XM_024452549.1:c.1350A>G	XP_024308317.1:p.Glu450=
XR_002958955.1:n.1923A>G
XR_002958956.1:n.1923A>G
XR_002958965.1:n.1814A>G
NM_006642.5:c.1881A>G MANE Select	NP_006633.1:p.Glu627=
NM_001350246.2:c.978A>G	NP_001337175.1:p.Glu326=
NM_001350247.2:c.978A>G	NP_001337176.1:p.Glu326=
NM_001350248.2:c.1977A>G	NP_001337177.1:p.Glu659=
NM_001350249.2:c.1587A>G	NP_001337178.1:p.Glu529=
NM_001350251.2:c.978A>G	NP_001337180.1:p.Glu326=