Canonical Allele Identifier: CA345667639

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589730T>G (hg19) ; chr1:g.243426428T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426428T>G , CM000663.2:g.243426428T>G	GRCh38
NC_000001.10:g.243589730T>G , CM000663.1:g.243589730T>G	GRCh37
NC_000001.9:g.241656353T>G	NCBI36
NG_027811.1:g.175424T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1855T>G MANE Select	ENSP00000355499.3:p.Ser619Ala
ENST00000366541.7:c.1855T>G	ENSP00000355499.3:p.Ser619Ala
ENST00000435549.1:c.958T>G	ENSP00000410200.1:p.Ser320Ala
ENST00000463042.1:n.62T>G
NM_006642.3:c.1855T>G	NP_006633.1:p.Ser619Ala
XM_005273013.3:c.1726T>G	XP_005273070.1:p.Ser576Ala
XM_005273018.1:c.1432T>G	XP_005273075.1:p.Ser478Ala
XM_005273021.3:c.952T>G	XP_005273078.1:p.Ser318Ala
XM_005273022.2:c.934T>G	XP_005273079.1:p.Ser312Ala
XM_006711727.2:c.1885T>G	XP_006711790.1:p.Ser629Ala
XM_006711728.2:c.1756T>G	XP_006711791.1:p.Ser586Ala
XM_006711729.2:c.1696T>G	XP_006711792.1:p.Ser566Ala
XM_011544021.1:c.1981T>G	XP_011542323.1:p.Ser661Ala
XM_011544022.1:c.1951T>G	XP_011542324.1:p.Ser651Ala
XM_011544023.1:c.1981T>G	XP_011542325.1:p.Ser661Ala
XM_011544024.1:c.1981T>G	XP_011542326.1:p.Ser661Ala
XM_011544025.1:c.1792T>G	XP_011542327.1:p.Ser598Ala
XM_011544026.1:c.1744T>G	XP_011542328.1:p.Ser582Ala
XM_011544027.1:c.1567T>G	XP_011542329.1:p.Ser523Ala
XM_011544028.1:c.1519T>G	XP_011542330.1:p.Ser507Ala
XM_011544030.1:c.910T>G	XP_011542332.1:p.Ser304Ala
XR_949128.1:n.2005T>G
NM_001350246.1:c.952T>G	NP_001337175.1:p.Ser318Ala
NM_001350247.1:c.952T>G	NP_001337176.1:p.Ser318Ala
NM_001350248.1:c.1951T>G	NP_001337177.1:p.Ser651Ala
NM_001350249.1:c.1561T>G	NP_001337178.1:p.Ser521Ala
NM_001350251.1:c.952T>G	NP_001337180.1:p.Ser318Ala
NM_006642.4:c.1855T>G	NP_006633.1:p.Ser619Ala
XM_005273013.5:c.1726T>G	XP_005273070.1:p.Ser576Ala
XM_005273018.2:c.1432T>G	XP_005273075.1:p.Ser478Ala
XM_005273022.4:c.934T>G	XP_005273079.1:p.Ser312Ala
XM_011544026.3:c.1744T>G	XP_011542328.1:p.Ser582Ala
XM_011544028.3:c.1519T>G	XP_011542330.1:p.Ser507Ala
XM_011544030.3:c.910T>G	XP_011542332.1:p.Ser304Ala
XM_017000104.2:c.1726T>G	XP_016855593.1:p.Ser576Ala
XM_017000105.2:c.1618T>G	XP_016855594.1:p.Ser540Ala
XM_024452537.1:c.1657T>G	XP_024308305.1:p.Ser553Ala
XM_024452539.1:c.1657T>G	XP_024308307.1:p.Ser553Ala
XM_024452540.1:c.1657T>G	XP_024308308.1:p.Ser553Ala
XM_024452547.1:c.1561T>G	XP_024308315.1:p.Ser521Ala
XM_024452548.1:c.1657T>G	XP_024308316.1:p.Ser553Ala
XM_024452549.1:c.1324T>G	XP_024308317.1:p.Ser442Ala
XR_002958955.1:n.1897T>G
XR_002958956.1:n.1897T>G
XR_002958965.1:n.1788T>G
NM_006642.5:c.1855T>G MANE Select	NP_006633.1:p.Ser619Ala
NM_001350246.2:c.952T>G	NP_001337175.1:p.Ser318Ala
NM_001350247.2:c.952T>G	NP_001337176.1:p.Ser318Ala
NM_001350248.2:c.1951T>G	NP_001337177.1:p.Ser651Ala
NM_001350249.2:c.1561T>G	NP_001337178.1:p.Ser521Ala
NM_001350251.2:c.952T>G	NP_001337180.1:p.Ser318Ala