Canonical Allele Identifier: CA345667735

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589773A>C (hg19) ; chr1:g.243426471A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426471A>C , CM000663.2:g.243426471A>C	GRCh38
NC_000001.10:g.243589773A>C , CM000663.1:g.243589773A>C	GRCh37
NC_000001.9:g.241656396A>C	NCBI36
NG_027811.1:g.175467A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1898A>C MANE Select	ENSP00000355499.3:p.Asp633Ala
ENST00000366541.7:c.1898A>C	ENSP00000355499.3:p.Asp633Ala
ENST00000435549.1:c.1001A>C	ENSP00000410200.1:p.Asp334Ala
ENST00000463042.1:n.105A>C
NM_006642.3:c.1898A>C	NP_006633.1:p.Asp633Ala
XM_005273013.3:c.1769A>C	XP_005273070.1:p.Asp590Ala
XM_005273018.1:c.1475A>C	XP_005273075.1:p.Asp492Ala
XM_005273021.3:c.995A>C	XP_005273078.1:p.Asp332Ala
XM_005273022.2:c.977A>C	XP_005273079.1:p.Asp326Ala
XM_006711727.2:c.1928A>C	XP_006711790.1:p.Asp643Ala
XM_006711728.2:c.1799A>C	XP_006711791.1:p.Asp600Ala
XM_006711729.2:c.1739A>C	XP_006711792.1:p.Asp580Ala
XM_011544021.1:c.2024A>C	XP_011542323.1:p.Asp675Ala
XM_011544022.1:c.1994A>C	XP_011542324.1:p.Asp665Ala
XM_011544023.1:c.2024A>C	XP_011542325.1:p.Asp675Ala
XM_011544024.1:c.2024A>C	XP_011542326.1:p.Asp675Ala
XM_011544025.1:c.1835A>C	XP_011542327.1:p.Asp612Ala
XM_011544026.1:c.1787A>C	XP_011542328.1:p.Asp596Ala
XM_011544027.1:c.1610A>C	XP_011542329.1:p.Asp537Ala
XM_011544028.1:c.1562A>C	XP_011542330.1:p.Asp521Ala
XM_011544030.1:c.953A>C	XP_011542332.1:p.Asp318Ala
XR_949128.1:n.2048A>C
NM_001350246.1:c.995A>C	NP_001337175.1:p.Asp332Ala
NM_001350247.1:c.995A>C	NP_001337176.1:p.Asp332Ala
NM_001350248.1:c.1994A>C	NP_001337177.1:p.Asp665Ala
NM_001350249.1:c.1604A>C	NP_001337178.1:p.Asp535Ala
NM_001350251.1:c.995A>C	NP_001337180.1:p.Asp332Ala
NM_006642.4:c.1898A>C	NP_006633.1:p.Asp633Ala
XM_005273013.5:c.1769A>C	XP_005273070.1:p.Asp590Ala
XM_005273018.2:c.1475A>C	XP_005273075.1:p.Asp492Ala
XM_005273022.4:c.977A>C	XP_005273079.1:p.Asp326Ala
XM_011544026.3:c.1787A>C	XP_011542328.1:p.Asp596Ala
XM_011544028.3:c.1562A>C	XP_011542330.1:p.Asp521Ala
XM_011544030.3:c.953A>C	XP_011542332.1:p.Asp318Ala
XM_017000104.2:c.1769A>C	XP_016855593.1:p.Asp590Ala
XM_017000105.2:c.1661A>C	XP_016855594.1:p.Asp554Ala
XM_024452537.1:c.1700A>C	XP_024308305.1:p.Asp567Ala
XM_024452539.1:c.1700A>C	XP_024308307.1:p.Asp567Ala
XM_024452540.1:c.1700A>C	XP_024308308.1:p.Asp567Ala
XM_024452547.1:c.1604A>C	XP_024308315.1:p.Asp535Ala
XM_024452548.1:c.1700A>C	XP_024308316.1:p.Asp567Ala
XM_024452549.1:c.1367A>C	XP_024308317.1:p.Asp456Ala
XR_002958955.1:n.1940A>C
XR_002958956.1:n.1940A>C
XR_002958965.1:n.1831A>C
NM_006642.5:c.1898A>C MANE Select	NP_006633.1:p.Asp633Ala
NM_001350246.2:c.995A>C	NP_001337175.1:p.Asp332Ala
NM_001350247.2:c.995A>C	NP_001337176.1:p.Asp332Ala
NM_001350248.2:c.1994A>C	NP_001337177.1:p.Asp665Ala
NM_001350249.2:c.1604A>C	NP_001337178.1:p.Asp535Ala
NM_001350251.2:c.995A>C	NP_001337180.1:p.Asp332Ala