Canonical Allele Identifier: CA424100932

Gene: SDCCAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243378774G>A , CM000663.2:g.243378774G>A	GRCh38
NC_000001.10:g.243542076G>A , CM000663.1:g.243542076G>A	GRCh37
NC_000001.9:g.241608699G>A	NCBI36
NG_027811.1:g.127770G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1527G>A MANE Select	ENSP00000355499.3:p.Gln509=
ENST00000366541.7:c.1527G>A	ENSP00000355499.3:p.Gln509=
ENST00000435549.1:c.867G>A	ENSP00000410200.1:p.Gln289=
ENST00000493334.1:n.494G>A
NM_006642.3:c.1527G>A	NP_006633.1:p.Gln509=
XM_005273013.3:c.1398G>A	XP_005273070.1:p.Gln466=
XM_005273018.1:c.1104G>A	XP_005273075.1:p.Gln368=
XM_005273021.3:c.624G>A	XP_005273078.1:p.Gln208=
XM_005273022.2:c.606G>A	XP_005273079.1:p.Gln202=
XM_006711727.2:c.1557G>A	XP_006711790.1:p.Gln519=
XM_006711728.2:c.1428G>A	XP_006711791.1:p.Gln476=
XM_006711729.2:c.1368G>A	XP_006711792.1:p.Gln456=
XM_011544021.1:c.1653G>A	XP_011542323.1:p.Gln551=
XM_011544022.1:c.1623G>A	XP_011542324.1:p.Gln541=
XM_011544023.1:c.1653G>A	XP_011542325.1:p.Gln551=
XM_011544024.1:c.1653G>A	XP_011542326.1:p.Gln551=
XM_011544025.1:c.1464G>A	XP_011542327.1:p.Gln488=
XM_011544026.1:c.1653G>A	XP_011542328.1:p.Gln551=
XM_011544027.1:c.1239G>A	XP_011542329.1:p.Gln413=
XM_011544028.1:c.1428G>A	XP_011542330.1:p.Gln476=
XM_011544030.1:c.582G>A	XP_011542332.1:p.Gln194=
XR_949128.1:n.1677G>A
NM_001350246.1:c.624G>A	NP_001337175.1:p.Gln208=
NM_001350247.1:c.624G>A	NP_001337176.1:p.Gln208=
NM_001350248.1:c.1623G>A	NP_001337177.1:p.Gln541=
NM_001350249.1:c.1233G>A	NP_001337178.1:p.Gln411=
NM_001350251.1:c.624G>A	NP_001337180.1:p.Gln208=
NM_006642.4:c.1527G>A	NP_006633.1:p.Gln509=
XM_005273013.5:c.1398G>A	XP_005273070.1:p.Gln466=
XM_005273018.2:c.1104G>A	XP_005273075.1:p.Gln368=
XM_005273022.4:c.606G>A	XP_005273079.1:p.Gln202=
XM_011544026.3:c.1653G>A	XP_011542328.1:p.Gln551=
XM_011544028.3:c.1428G>A	XP_011542330.1:p.Gln476=
XM_011544030.3:c.582G>A	XP_011542332.1:p.Gln194=
XM_017000104.2:c.1398G>A	XP_016855593.1:p.Gln466=
XM_017000105.2:c.1527G>A	XP_016855594.1:p.Gln509=
XM_024452537.1:c.1329G>A	XP_024308305.1:p.Gln443=
XM_024452539.1:c.1329G>A	XP_024308307.1:p.Gln443=
XM_024452540.1:c.1329G>A	XP_024308308.1:p.Gln443=
XM_024452547.1:c.1233G>A	XP_024308315.1:p.Gln411=
XM_024452548.1:c.1329G>A	XP_024308316.1:p.Gln443=
XM_024452549.1:c.1233G>A	XP_024308317.1:p.Gln411=
XR_002958955.1:n.1569G>A
XR_002958956.1:n.1569G>A
XR_002958965.1:n.1569G>A
NM_006642.5:c.1527G>A MANE Select	NP_006633.1:p.Gln509=
NM_001350246.2:c.624G>A	NP_001337175.1:p.Gln208=
NM_001350247.2:c.624G>A	NP_001337176.1:p.Gln208=
NM_001350248.2:c.1623G>A	NP_001337177.1:p.Gln541=
NM_001350249.2:c.1233G>A	NP_001337178.1:p.Gln411=
NM_001350251.2:c.624G>A	NP_001337180.1:p.Gln208=