Canonical Allele Identifier: CA345667884

Gene: SDCCAG8

Linked Data

• gnomAD v4: 1-243426534-G-A
• MyVariant Identifiers: chr1:g.243589836G>A (hg19) ; chr1:g.243426534G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426534G>A , CM000663.2:g.243426534G>A	GRCh38
NC_000001.10:g.243589836G>A , CM000663.1:g.243589836G>A	GRCh37
NC_000001.9:g.241656459G>A	NCBI36
NG_027811.1:g.175530G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1961G>A MANE Select	ENSP00000355499.3:p.Arg654Lys
ENST00000366541.7:c.1961G>A	ENSP00000355499.3:p.Arg654Lys
ENST00000435549.1:c.1064G>A	ENSP00000410200.1:p.Arg355Lys
ENST00000463042.1:n.168G>A
NM_006642.3:c.1961G>A	NP_006633.1:p.Arg654Lys
XM_005273013.3:c.1832G>A	XP_005273070.1:p.Arg611Lys
XM_005273018.1:c.1538G>A	XP_005273075.1:p.Arg513Lys
XM_005273021.3:c.1058G>A	XP_005273078.1:p.Arg353Lys
XM_005273022.2:c.1040G>A	XP_005273079.1:p.Arg347Lys
XM_006711727.2:c.1991G>A	XP_006711790.1:p.Arg664Lys
XM_006711728.2:c.1862G>A	XP_006711791.1:p.Arg621Lys
XM_006711729.2:c.1802G>A	XP_006711792.1:p.Arg601Lys
XM_011544021.1:c.2087G>A	XP_011542323.1:p.Arg696Lys
XM_011544022.1:c.2057G>A	XP_011542324.1:p.Arg686Lys
XM_011544023.1:c.2087G>A	XP_011542325.1:p.Arg696Lys
XM_011544024.1:c.2087G>A	XP_011542326.1:p.Arg696Lys
XM_011544025.1:c.1898G>A	XP_011542327.1:p.Arg633Lys
XM_011544026.1:c.1850G>A	XP_011542328.1:p.Arg617Lys
XM_011544027.1:c.1673G>A	XP_011542329.1:p.Arg558Lys
XM_011544028.1:c.1625G>A	XP_011542330.1:p.Arg542Lys
XM_011544030.1:c.1016G>A	XP_011542332.1:p.Arg339Lys
XR_949128.1:n.2111G>A
NM_001350246.1:c.1058G>A	NP_001337175.1:p.Arg353Lys
NM_001350247.1:c.1058G>A	NP_001337176.1:p.Arg353Lys
NM_001350248.1:c.2057G>A	NP_001337177.1:p.Arg686Lys
NM_001350249.1:c.1667G>A	NP_001337178.1:p.Arg556Lys
NM_001350251.1:c.1058G>A	NP_001337180.1:p.Arg353Lys
NM_006642.4:c.1961G>A	NP_006633.1:p.Arg654Lys
XM_005273013.5:c.1832G>A	XP_005273070.1:p.Arg611Lys
XM_005273018.2:c.1538G>A	XP_005273075.1:p.Arg513Lys
XM_005273022.4:c.1040G>A	XP_005273079.1:p.Arg347Lys
XM_011544026.3:c.1850G>A	XP_011542328.1:p.Arg617Lys
XM_011544028.3:c.1625G>A	XP_011542330.1:p.Arg542Lys
XM_011544030.3:c.1016G>A	XP_011542332.1:p.Arg339Lys
XM_017000104.2:c.1832G>A	XP_016855593.1:p.Arg611Lys
XM_017000105.2:c.1724G>A	XP_016855594.1:p.Arg575Lys
XM_024452537.1:c.1763G>A	XP_024308305.1:p.Arg588Lys
XM_024452539.1:c.1763G>A	XP_024308307.1:p.Arg588Lys
XM_024452540.1:c.1763G>A	XP_024308308.1:p.Arg588Lys
XM_024452547.1:c.1667G>A	XP_024308315.1:p.Arg556Lys
XM_024452548.1:c.1763G>A	XP_024308316.1:p.Arg588Lys
XM_024452549.1:c.1430G>A	XP_024308317.1:p.Arg477Lys
XR_002958955.1:n.2003G>A
XR_002958956.1:n.2003G>A
XR_002958965.1:n.1894G>A
NM_006642.5:c.1961G>A MANE Select	NP_006633.1:p.Arg654Lys
NM_001350246.2:c.1058G>A	NP_001337175.1:p.Arg353Lys
NM_001350247.2:c.1058G>A	NP_001337176.1:p.Arg353Lys
NM_001350248.2:c.2057G>A	NP_001337177.1:p.Arg686Lys
NM_001350249.2:c.1667G>A	NP_001337178.1:p.Arg556Lys
NM_001350251.2:c.1058G>A	NP_001337180.1:p.Arg353Lys