Canonical Allele Identifier: CA345667863

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589827A>G (hg19) ; chr1:g.243426525A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426525A>G , CM000663.2:g.243426525A>G	GRCh38
NC_000001.10:g.243589827A>G , CM000663.1:g.243589827A>G	GRCh37
NC_000001.9:g.241656450A>G	NCBI36
NG_027811.1:g.175521A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1952A>G MANE Select	ENSP00000355499.3:p.Gln651Arg
ENST00000366541.7:c.1952A>G	ENSP00000355499.3:p.Gln651Arg
ENST00000435549.1:c.1055A>G	ENSP00000410200.1:p.Gln352Arg
ENST00000463042.1:n.159A>G
NM_006642.3:c.1952A>G	NP_006633.1:p.Gln651Arg
XM_005273013.3:c.1823A>G	XP_005273070.1:p.Gln608Arg
XM_005273018.1:c.1529A>G	XP_005273075.1:p.Gln510Arg
XM_005273021.3:c.1049A>G	XP_005273078.1:p.Gln350Arg
XM_005273022.2:c.1031A>G	XP_005273079.1:p.Gln344Arg
XM_006711727.2:c.1982A>G	XP_006711790.1:p.Gln661Arg
XM_006711728.2:c.1853A>G	XP_006711791.1:p.Gln618Arg
XM_006711729.2:c.1793A>G	XP_006711792.1:p.Gln598Arg
XM_011544021.1:c.2078A>G	XP_011542323.1:p.Gln693Arg
XM_011544022.1:c.2048A>G	XP_011542324.1:p.Gln683Arg
XM_011544023.1:c.2078A>G	XP_011542325.1:p.Gln693Arg
XM_011544024.1:c.2078A>G	XP_011542326.1:p.Gln693Arg
XM_011544025.1:c.1889A>G	XP_011542327.1:p.Gln630Arg
XM_011544026.1:c.1841A>G	XP_011542328.1:p.Gln614Arg
XM_011544027.1:c.1664A>G	XP_011542329.1:p.Gln555Arg
XM_011544028.1:c.1616A>G	XP_011542330.1:p.Gln539Arg
XM_011544030.1:c.1007A>G	XP_011542332.1:p.Gln336Arg
XR_949128.1:n.2102A>G
NM_001350246.1:c.1049A>G	NP_001337175.1:p.Gln350Arg
NM_001350247.1:c.1049A>G	NP_001337176.1:p.Gln350Arg
NM_001350248.1:c.2048A>G	NP_001337177.1:p.Gln683Arg
NM_001350249.1:c.1658A>G	NP_001337178.1:p.Gln553Arg
NM_001350251.1:c.1049A>G	NP_001337180.1:p.Gln350Arg
NM_006642.4:c.1952A>G	NP_006633.1:p.Gln651Arg
XM_005273013.5:c.1823A>G	XP_005273070.1:p.Gln608Arg
XM_005273018.2:c.1529A>G	XP_005273075.1:p.Gln510Arg
XM_005273022.4:c.1031A>G	XP_005273079.1:p.Gln344Arg
XM_011544026.3:c.1841A>G	XP_011542328.1:p.Gln614Arg
XM_011544028.3:c.1616A>G	XP_011542330.1:p.Gln539Arg
XM_011544030.3:c.1007A>G	XP_011542332.1:p.Gln336Arg
XM_017000104.2:c.1823A>G	XP_016855593.1:p.Gln608Arg
XM_017000105.2:c.1715A>G	XP_016855594.1:p.Gln572Arg
XM_024452537.1:c.1754A>G	XP_024308305.1:p.Gln585Arg
XM_024452539.1:c.1754A>G	XP_024308307.1:p.Gln585Arg
XM_024452540.1:c.1754A>G	XP_024308308.1:p.Gln585Arg
XM_024452547.1:c.1658A>G	XP_024308315.1:p.Gln553Arg
XM_024452548.1:c.1754A>G	XP_024308316.1:p.Gln585Arg
XM_024452549.1:c.1421A>G	XP_024308317.1:p.Gln474Arg
XR_002958955.1:n.1994A>G
XR_002958956.1:n.1994A>G
XR_002958965.1:n.1885A>G
NM_006642.5:c.1952A>G MANE Select	NP_006633.1:p.Gln651Arg
NM_001350246.2:c.1049A>G	NP_001337175.1:p.Gln350Arg
NM_001350247.2:c.1049A>G	NP_001337176.1:p.Gln350Arg
NM_001350248.2:c.2048A>G	NP_001337177.1:p.Gln683Arg
NM_001350249.2:c.1658A>G	NP_001337178.1:p.Gln553Arg
NM_001350251.2:c.1049A>G	NP_001337180.1:p.Gln350Arg