Canonical Allele Identifier: CA345667658

Gene: SDCCAG8

Linked Data

• MyVariant Identifiers: chr1:g.243589739G>A (hg19) ; chr1:g.243426437G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426437G>A , CM000663.2:g.243426437G>A	GRCh38
NC_000001.10:g.243589739G>A , CM000663.1:g.243589739G>A	GRCh37
NC_000001.9:g.241656362G>A	NCBI36
NG_027811.1:g.175433G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1864G>A MANE Select	ENSP00000355499.3:p.Ala622Thr
ENST00000366541.7:c.1864G>A	ENSP00000355499.3:p.Ala622Thr
ENST00000435549.1:c.967G>A	ENSP00000410200.1:p.Ala323Thr
ENST00000463042.1:n.71G>A
NM_006642.3:c.1864G>A	NP_006633.1:p.Ala622Thr
XM_005273013.3:c.1735G>A	XP_005273070.1:p.Ala579Thr
XM_005273018.1:c.1441G>A	XP_005273075.1:p.Ala481Thr
XM_005273021.3:c.961G>A	XP_005273078.1:p.Ala321Thr
XM_005273022.2:c.943G>A	XP_005273079.1:p.Ala315Thr
XM_006711727.2:c.1894G>A	XP_006711790.1:p.Ala632Thr
XM_006711728.2:c.1765G>A	XP_006711791.1:p.Ala589Thr
XM_006711729.2:c.1705G>A	XP_006711792.1:p.Ala569Thr
XM_011544021.1:c.1990G>A	XP_011542323.1:p.Ala664Thr
XM_011544022.1:c.1960G>A	XP_011542324.1:p.Ala654Thr
XM_011544023.1:c.1990G>A	XP_011542325.1:p.Ala664Thr
XM_011544024.1:c.1990G>A	XP_011542326.1:p.Ala664Thr
XM_011544025.1:c.1801G>A	XP_011542327.1:p.Ala601Thr
XM_011544026.1:c.1753G>A	XP_011542328.1:p.Ala585Thr
XM_011544027.1:c.1576G>A	XP_011542329.1:p.Ala526Thr
XM_011544028.1:c.1528G>A	XP_011542330.1:p.Ala510Thr
XM_011544030.1:c.919G>A	XP_011542332.1:p.Ala307Thr
XR_949128.1:n.2014G>A
NM_001350246.1:c.961G>A	NP_001337175.1:p.Ala321Thr
NM_001350247.1:c.961G>A	NP_001337176.1:p.Ala321Thr
NM_001350248.1:c.1960G>A	NP_001337177.1:p.Ala654Thr
NM_001350249.1:c.1570G>A	NP_001337178.1:p.Ala524Thr
NM_001350251.1:c.961G>A	NP_001337180.1:p.Ala321Thr
NM_006642.4:c.1864G>A	NP_006633.1:p.Ala622Thr
XM_005273013.5:c.1735G>A	XP_005273070.1:p.Ala579Thr
XM_005273018.2:c.1441G>A	XP_005273075.1:p.Ala481Thr
XM_005273022.4:c.943G>A	XP_005273079.1:p.Ala315Thr
XM_011544026.3:c.1753G>A	XP_011542328.1:p.Ala585Thr
XM_011544028.3:c.1528G>A	XP_011542330.1:p.Ala510Thr
XM_011544030.3:c.919G>A	XP_011542332.1:p.Ala307Thr
XM_017000104.2:c.1735G>A	XP_016855593.1:p.Ala579Thr
XM_017000105.2:c.1627G>A	XP_016855594.1:p.Ala543Thr
XM_024452537.1:c.1666G>A	XP_024308305.1:p.Ala556Thr
XM_024452539.1:c.1666G>A	XP_024308307.1:p.Ala556Thr
XM_024452540.1:c.1666G>A	XP_024308308.1:p.Ala556Thr
XM_024452547.1:c.1570G>A	XP_024308315.1:p.Ala524Thr
XM_024452548.1:c.1666G>A	XP_024308316.1:p.Ala556Thr
XM_024452549.1:c.1333G>A	XP_024308317.1:p.Ala445Thr
XR_002958955.1:n.1906G>A
XR_002958956.1:n.1906G>A
XR_002958965.1:n.1797G>A
NM_006642.5:c.1864G>A MANE Select	NP_006633.1:p.Ala622Thr
NM_001350246.2:c.961G>A	NP_001337175.1:p.Ala321Thr
NM_001350247.2:c.961G>A	NP_001337176.1:p.Ala321Thr
NM_001350248.2:c.1960G>A	NP_001337177.1:p.Ala654Thr
NM_001350249.2:c.1570G>A	NP_001337178.1:p.Ala524Thr
NM_001350251.2:c.961G>A	NP_001337180.1:p.Ala321Thr