Canonical Allele Identifier: CA345667852

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589822T>G (hg19) ; chr1:g.243426520T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426520T>G , CM000663.2:g.243426520T>G	GRCh38
NC_000001.10:g.243589822T>G , CM000663.1:g.243589822T>G	GRCh37
NC_000001.9:g.241656445T>G	NCBI36
NG_027811.1:g.175516T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1947T>G MANE Select	ENSP00000355499.3:p.Cys649Trp
ENST00000366541.7:c.1947T>G	ENSP00000355499.3:p.Cys649Trp
ENST00000435549.1:c.1050T>G	ENSP00000410200.1:p.Cys350Trp
ENST00000463042.1:n.154T>G
NM_006642.3:c.1947T>G	NP_006633.1:p.Cys649Trp
XM_005273013.3:c.1818T>G	XP_005273070.1:p.Cys606Trp
XM_005273018.1:c.1524T>G	XP_005273075.1:p.Cys508Trp
XM_005273021.3:c.1044T>G	XP_005273078.1:p.Cys348Trp
XM_005273022.2:c.1026T>G	XP_005273079.1:p.Cys342Trp
XM_006711727.2:c.1977T>G	XP_006711790.1:p.Cys659Trp
XM_006711728.2:c.1848T>G	XP_006711791.1:p.Cys616Trp
XM_006711729.2:c.1788T>G	XP_006711792.1:p.Cys596Trp
XM_011544021.1:c.2073T>G	XP_011542323.1:p.Cys691Trp
XM_011544022.1:c.2043T>G	XP_011542324.1:p.Cys681Trp
XM_011544023.1:c.2073T>G	XP_011542325.1:p.Cys691Trp
XM_011544024.1:c.2073T>G	XP_011542326.1:p.Cys691Trp
XM_011544025.1:c.1884T>G	XP_011542327.1:p.Cys628Trp
XM_011544026.1:c.1836T>G	XP_011542328.1:p.Cys612Trp
XM_011544027.1:c.1659T>G	XP_011542329.1:p.Cys553Trp
XM_011544028.1:c.1611T>G	XP_011542330.1:p.Cys537Trp
XM_011544030.1:c.1002T>G	XP_011542332.1:p.Cys334Trp
XR_949128.1:n.2097T>G
NM_001350246.1:c.1044T>G	NP_001337175.1:p.Cys348Trp
NM_001350247.1:c.1044T>G	NP_001337176.1:p.Cys348Trp
NM_001350248.1:c.2043T>G	NP_001337177.1:p.Cys681Trp
NM_001350249.1:c.1653T>G	NP_001337178.1:p.Cys551Trp
NM_001350251.1:c.1044T>G	NP_001337180.1:p.Cys348Trp
NM_006642.4:c.1947T>G	NP_006633.1:p.Cys649Trp
XM_005273013.5:c.1818T>G	XP_005273070.1:p.Cys606Trp
XM_005273018.2:c.1524T>G	XP_005273075.1:p.Cys508Trp
XM_005273022.4:c.1026T>G	XP_005273079.1:p.Cys342Trp
XM_011544026.3:c.1836T>G	XP_011542328.1:p.Cys612Trp
XM_011544028.3:c.1611T>G	XP_011542330.1:p.Cys537Trp
XM_011544030.3:c.1002T>G	XP_011542332.1:p.Cys334Trp
XM_017000104.2:c.1818T>G	XP_016855593.1:p.Cys606Trp
XM_017000105.2:c.1710T>G	XP_016855594.1:p.Cys570Trp
XM_024452537.1:c.1749T>G	XP_024308305.1:p.Cys583Trp
XM_024452539.1:c.1749T>G	XP_024308307.1:p.Cys583Trp
XM_024452540.1:c.1749T>G	XP_024308308.1:p.Cys583Trp
XM_024452547.1:c.1653T>G	XP_024308315.1:p.Cys551Trp
XM_024452548.1:c.1749T>G	XP_024308316.1:p.Cys583Trp
XM_024452549.1:c.1416T>G	XP_024308317.1:p.Cys472Trp
XR_002958955.1:n.1989T>G
XR_002958956.1:n.1989T>G
XR_002958965.1:n.1880T>G
NM_006642.5:c.1947T>G MANE Select	NP_006633.1:p.Cys649Trp
NM_001350246.2:c.1044T>G	NP_001337175.1:p.Cys348Trp
NM_001350247.2:c.1044T>G	NP_001337176.1:p.Cys348Trp
NM_001350248.2:c.2043T>G	NP_001337177.1:p.Cys681Trp
NM_001350249.2:c.1653T>G	NP_001337178.1:p.Cys551Trp
NM_001350251.2:c.1044T>G	NP_001337180.1:p.Cys348Trp