Canonical Allele Identifier: CA345667652

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589736A>G (hg19) ; chr1:g.243426434A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426434A>G , CM000663.2:g.243426434A>G	GRCh38
NC_000001.10:g.243589736A>G , CM000663.1:g.243589736A>G	GRCh37
NC_000001.9:g.241656359A>G	NCBI36
NG_027811.1:g.175430A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1861A>G MANE Select	ENSP00000355499.3:p.Ile621Val
ENST00000366541.7:c.1861A>G	ENSP00000355499.3:p.Ile621Val
ENST00000435549.1:c.964A>G	ENSP00000410200.1:p.Ile322Val
ENST00000463042.1:n.68A>G
NM_006642.3:c.1861A>G	NP_006633.1:p.Ile621Val
XM_005273013.3:c.1732A>G	XP_005273070.1:p.Ile578Val
XM_005273018.1:c.1438A>G	XP_005273075.1:p.Ile480Val
XM_005273021.3:c.958A>G	XP_005273078.1:p.Ile320Val
XM_005273022.2:c.940A>G	XP_005273079.1:p.Ile314Val
XM_006711727.2:c.1891A>G	XP_006711790.1:p.Ile631Val
XM_006711728.2:c.1762A>G	XP_006711791.1:p.Ile588Val
XM_006711729.2:c.1702A>G	XP_006711792.1:p.Ile568Val
XM_011544021.1:c.1987A>G	XP_011542323.1:p.Ile663Val
XM_011544022.1:c.1957A>G	XP_011542324.1:p.Ile653Val
XM_011544023.1:c.1987A>G	XP_011542325.1:p.Ile663Val
XM_011544024.1:c.1987A>G	XP_011542326.1:p.Ile663Val
XM_011544025.1:c.1798A>G	XP_011542327.1:p.Ile600Val
XM_011544026.1:c.1750A>G	XP_011542328.1:p.Ile584Val
XM_011544027.1:c.1573A>G	XP_011542329.1:p.Ile525Val
XM_011544028.1:c.1525A>G	XP_011542330.1:p.Ile509Val
XM_011544030.1:c.916A>G	XP_011542332.1:p.Ile306Val
XR_949128.1:n.2011A>G
NM_001350246.1:c.958A>G	NP_001337175.1:p.Ile320Val
NM_001350247.1:c.958A>G	NP_001337176.1:p.Ile320Val
NM_001350248.1:c.1957A>G	NP_001337177.1:p.Ile653Val
NM_001350249.1:c.1567A>G	NP_001337178.1:p.Ile523Val
NM_001350251.1:c.958A>G	NP_001337180.1:p.Ile320Val
NM_006642.4:c.1861A>G	NP_006633.1:p.Ile621Val
XM_005273013.5:c.1732A>G	XP_005273070.1:p.Ile578Val
XM_005273018.2:c.1438A>G	XP_005273075.1:p.Ile480Val
XM_005273022.4:c.940A>G	XP_005273079.1:p.Ile314Val
XM_011544026.3:c.1750A>G	XP_011542328.1:p.Ile584Val
XM_011544028.3:c.1525A>G	XP_011542330.1:p.Ile509Val
XM_011544030.3:c.916A>G	XP_011542332.1:p.Ile306Val
XM_017000104.2:c.1732A>G	XP_016855593.1:p.Ile578Val
XM_017000105.2:c.1624A>G	XP_016855594.1:p.Ile542Val
XM_024452537.1:c.1663A>G	XP_024308305.1:p.Ile555Val
XM_024452539.1:c.1663A>G	XP_024308307.1:p.Ile555Val
XM_024452540.1:c.1663A>G	XP_024308308.1:p.Ile555Val
XM_024452547.1:c.1567A>G	XP_024308315.1:p.Ile523Val
XM_024452548.1:c.1663A>G	XP_024308316.1:p.Ile555Val
XM_024452549.1:c.1330A>G	XP_024308317.1:p.Ile444Val
XR_002958955.1:n.1903A>G
XR_002958956.1:n.1903A>G
XR_002958965.1:n.1794A>G
NM_006642.5:c.1861A>G MANE Select	NP_006633.1:p.Ile621Val
NM_001350246.2:c.958A>G	NP_001337175.1:p.Ile320Val
NM_001350247.2:c.958A>G	NP_001337176.1:p.Ile320Val
NM_001350248.2:c.1957A>G	NP_001337177.1:p.Ile653Val
NM_001350249.2:c.1567A>G	NP_001337178.1:p.Ile523Val
NM_001350251.2:c.958A>G	NP_001337180.1:p.Ile320Val