Canonical Allele Identifier: CA41009608

Gene: SDCCAG8

Linked Data

• dbSNP Id: rs1012914757
• gnomAD v2: 1-243589799-A-G
• gnomAD v4: 1-243426497-A-G
• MyVariant Identifiers: chr1:g.243589799A>G (hg19) ; chr1:g.243426497A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426497A>G , CM000663.2:g.243426497A>G	GRCh38
NC_000001.10:g.243589799A>G , CM000663.1:g.243589799A>G	GRCh37
NC_000001.9:g.241656422A>G	NCBI36
NG_027811.1:g.175493A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1924A>G MANE Select	ENSP00000355499.3:p.Asn642Asp
ENST00000366541.7:c.1924A>G	ENSP00000355499.3:p.Asn642Asp
ENST00000435549.1:c.1027A>G	ENSP00000410200.1:p.Asn343Asp
ENST00000463042.1:n.131A>G
NM_006642.3:c.1924A>G	NP_006633.1:p.Asn642Asp
XM_005273013.3:c.1795A>G	XP_005273070.1:p.Asn599Asp
XM_005273018.1:c.1501A>G	XP_005273075.1:p.Asn501Asp
XM_005273021.3:c.1021A>G	XP_005273078.1:p.Asn341Asp
XM_005273022.2:c.1003A>G	XP_005273079.1:p.Asn335Asp
XM_006711727.2:c.1954A>G	XP_006711790.1:p.Asn652Asp
XM_006711728.2:c.1825A>G	XP_006711791.1:p.Asn609Asp
XM_006711729.2:c.1765A>G	XP_006711792.1:p.Asn589Asp
XM_011544021.1:c.2050A>G	XP_011542323.1:p.Asn684Asp
XM_011544022.1:c.2020A>G	XP_011542324.1:p.Asn674Asp
XM_011544023.1:c.2050A>G	XP_011542325.1:p.Asn684Asp
XM_011544024.1:c.2050A>G	XP_011542326.1:p.Asn684Asp
XM_011544025.1:c.1861A>G	XP_011542327.1:p.Asn621Asp
XM_011544026.1:c.1813A>G	XP_011542328.1:p.Asn605Asp
XM_011544027.1:c.1636A>G	XP_011542329.1:p.Asn546Asp
XM_011544028.1:c.1588A>G	XP_011542330.1:p.Asn530Asp
XM_011544030.1:c.979A>G	XP_011542332.1:p.Asn327Asp
XR_949128.1:n.2074A>G
NM_001350246.1:c.1021A>G	NP_001337175.1:p.Asn341Asp
NM_001350247.1:c.1021A>G	NP_001337176.1:p.Asn341Asp
NM_001350248.1:c.2020A>G	NP_001337177.1:p.Asn674Asp
NM_001350249.1:c.1630A>G	NP_001337178.1:p.Asn544Asp
NM_001350251.1:c.1021A>G	NP_001337180.1:p.Asn341Asp
NM_006642.4:c.1924A>G	NP_006633.1:p.Asn642Asp
XM_005273013.5:c.1795A>G	XP_005273070.1:p.Asn599Asp
XM_005273018.2:c.1501A>G	XP_005273075.1:p.Asn501Asp
XM_005273022.4:c.1003A>G	XP_005273079.1:p.Asn335Asp
XM_011544026.3:c.1813A>G	XP_011542328.1:p.Asn605Asp
XM_011544028.3:c.1588A>G	XP_011542330.1:p.Asn530Asp
XM_011544030.3:c.979A>G	XP_011542332.1:p.Asn327Asp
XM_017000104.2:c.1795A>G	XP_016855593.1:p.Asn599Asp
XM_017000105.2:c.1687A>G	XP_016855594.1:p.Asn563Asp
XM_024452537.1:c.1726A>G	XP_024308305.1:p.Asn576Asp
XM_024452539.1:c.1726A>G	XP_024308307.1:p.Asn576Asp
XM_024452540.1:c.1726A>G	XP_024308308.1:p.Asn576Asp
XM_024452547.1:c.1630A>G	XP_024308315.1:p.Asn544Asp
XM_024452548.1:c.1726A>G	XP_024308316.1:p.Asn576Asp
XM_024452549.1:c.1393A>G	XP_024308317.1:p.Asn465Asp
XR_002958955.1:n.1966A>G
XR_002958956.1:n.1966A>G
XR_002958965.1:n.1857A>G
NM_006642.5:c.1924A>G MANE Select	NP_006633.1:p.Asn642Asp
NM_001350246.2:c.1021A>G	NP_001337175.1:p.Asn341Asp
NM_001350247.2:c.1021A>G	NP_001337176.1:p.Asn341Asp
NM_001350248.2:c.2020A>G	NP_001337177.1:p.Asn674Asp
NM_001350249.2:c.1630A>G	NP_001337178.1:p.Asn544Asp
NM_001350251.2:c.1021A>G	NP_001337180.1:p.Asn341Asp