Canonical Allele Identifier: CA345667660

Gene: SDCCAG8

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1864G>T MANE Select	ENSP00000355499.3:p.Ala622Ser
ENST00000366541.7:c.1864G>T	ENSP00000355499.3:p.Ala622Ser
ENST00000435549.1:c.967G>T	ENSP00000410200.1:p.Ala323Ser
ENST00000463042.1:n.71G>T
NM_006642.3:c.1864G>T	NP_006633.1:p.Ala622Ser
XM_005273013.3:c.1735G>T	XP_005273070.1:p.Ala579Ser
XM_005273018.1:c.1441G>T	XP_005273075.1:p.Ala481Ser
XM_005273021.3:c.961G>T	XP_005273078.1:p.Ala321Ser
XM_005273022.2:c.943G>T	XP_005273079.1:p.Ala315Ser
XM_006711727.2:c.1894G>T	XP_006711790.1:p.Ala632Ser
XM_006711728.2:c.1765G>T	XP_006711791.1:p.Ala589Ser
XM_006711729.2:c.1705G>T	XP_006711792.1:p.Ala569Ser
XM_011544021.1:c.1990G>T	XP_011542323.1:p.Ala664Ser
XM_011544022.1:c.1960G>T	XP_011542324.1:p.Ala654Ser
XM_011544023.1:c.1990G>T	XP_011542325.1:p.Ala664Ser
XM_011544024.1:c.1990G>T	XP_011542326.1:p.Ala664Ser
XM_011544025.1:c.1801G>T	XP_011542327.1:p.Ala601Ser
XM_011544026.1:c.1753G>T	XP_011542328.1:p.Ala585Ser
XM_011544027.1:c.1576G>T	XP_011542329.1:p.Ala526Ser
XM_011544028.1:c.1528G>T	XP_011542330.1:p.Ala510Ser
XM_011544030.1:c.919G>T	XP_011542332.1:p.Ala307Ser
XR_949128.1:n.2014G>T
NM_001350246.1:c.961G>T	NP_001337175.1:p.Ala321Ser
NM_001350247.1:c.961G>T	NP_001337176.1:p.Ala321Ser
NM_001350248.1:c.1960G>T	NP_001337177.1:p.Ala654Ser
NM_001350249.1:c.1570G>T	NP_001337178.1:p.Ala524Ser
NM_001350251.1:c.961G>T	NP_001337180.1:p.Ala321Ser
NM_006642.4:c.1864G>T	NP_006633.1:p.Ala622Ser
XM_005273013.5:c.1735G>T	XP_005273070.1:p.Ala579Ser
XM_005273018.2:c.1441G>T	XP_005273075.1:p.Ala481Ser
XM_005273022.4:c.943G>T	XP_005273079.1:p.Ala315Ser
XM_011544026.3:c.1753G>T	XP_011542328.1:p.Ala585Ser
XM_011544028.3:c.1528G>T	XP_011542330.1:p.Ala510Ser
XM_011544030.3:c.919G>T	XP_011542332.1:p.Ala307Ser
XM_017000104.2:c.1735G>T	XP_016855593.1:p.Ala579Ser
XM_017000105.2:c.1627G>T	XP_016855594.1:p.Ala543Ser
XM_024452537.1:c.1666G>T	XP_024308305.1:p.Ala556Ser
XM_024452539.1:c.1666G>T	XP_024308307.1:p.Ala556Ser
XM_024452540.1:c.1666G>T	XP_024308308.1:p.Ala556Ser
XM_024452547.1:c.1570G>T	XP_024308315.1:p.Ala524Ser
XM_024452548.1:c.1666G>T	XP_024308316.1:p.Ala556Ser
XM_024452549.1:c.1333G>T	XP_024308317.1:p.Ala445Ser
XR_002958955.1:n.1906G>T
XR_002958956.1:n.1906G>T
XR_002958965.1:n.1797G>T
NM_006642.5:c.1864G>T MANE Select	NP_006633.1:p.Ala622Ser
NM_001350246.2:c.961G>T	NP_001337175.1:p.Ala321Ser
NM_001350247.2:c.961G>T	NP_001337176.1:p.Ala321Ser
NM_001350248.2:c.1960G>T	NP_001337177.1:p.Ala654Ser
NM_001350249.2:c.1570G>T	NP_001337178.1:p.Ala524Ser
NM_001350251.2:c.961G>T	NP_001337180.1:p.Ala321Ser