Canonical Allele Identifier: CA1483406

Gene: SDCCAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243304733T>G , CM000663.2:g.243304733T>G	GRCh38
NC_000001.10:g.243468035T>G , CM000663.1:g.243468035T>G	GRCh37
NC_000001.9:g.241534658T>G	NCBI36
NG_027811.1:g.53729T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006642.5:c.696T>G MANE Select	NP_006633.1:p.Tyr232Ter
ENST00000366541.8:c.696T>G MANE Select	ENSP00000355499.3:p.Tyr232Ter
NM_001350246.1:c.-417T>G	NP_001337175.1:n.-417T>G
NM_001350246.2:c.-417T>G	NP_001337175.1:n.-417T>G
NM_001350247.1:c.-305T>G	NP_001337176.1:n.-305T>G
NM_001350247.2:c.-305T>G	NP_001337176.1:n.-305T>G
NM_001350248.1:c.792T>G	NP_001337177.1:p.Tyr264Ter
NM_001350248.2:c.792T>G	NP_001337177.1:p.Tyr264Ter
NM_001350249.1:c.402T>G	NP_001337178.1:p.Tyr134Ter
NM_001350249.2:c.402T>G	NP_001337178.1:p.Tyr134Ter
NM_001350251.1:c.-582T>G	NP_001337180.1:n.-582T>G
NM_001350251.2:c.-582T>G	NP_001337180.1:n.-582T>G
NM_006642.3:c.696T>G	NP_006633.1:p.Tyr232Ter
NM_006642.4:c.696T>G	NP_006633.1:p.Tyr232Ter
ENST00000366541.7:c.696T>G	ENSP00000355499.3:p.Tyr232Ter
ENST00000435549.1:c.36T>G	ENSP00000410200.1:p.Tyr12Ter
ENST00000476722.6:c.290T>G
ENST00000482234.1:n.429T>G
ENST00000496361.1:n.123T>G
XM_005273013.3:c.567T>G	XP_005273070.1:p.Tyr189Ter
XM_005273013.5:c.567T>G	XP_005273070.1:p.Tyr189Ter
XM_005273018.1:c.273T>G	XP_005273075.1:p.Tyr91Ter
XM_005273018.2:c.273T>G	XP_005273075.1:p.Tyr91Ter
XM_005273022.2:c.9-12022T>G	XP_005273079.1:n.9-12022T>G
XM_005273022.4:c.9-12022T>G	XP_005273079.1:n.9-12022T>G
XM_005273023.3:c.696T>G	XP_005273080.1:p.Tyr232Ter
XM_005273023.5:c.696T>G	XP_005273080.1:p.Tyr232Ter
XM_006711727.2:c.726T>G	XP_006711790.1:p.Tyr242Ter
XM_006711728.2:c.597T>G	XP_006711791.1:p.Tyr199Ter
XM_006711729.2:c.726T>G	XP_006711792.1:p.Tyr242Ter
XM_011544021.1:c.822T>G	XP_011542323.1:p.Tyr274Ter
XM_011544022.1:c.792T>G	XP_011542324.1:p.Tyr264Ter
XM_011544023.1:c.822T>G	XP_011542325.1:p.Tyr274Ter
XM_011544024.1:c.822T>G	XP_011542326.1:p.Tyr274Ter
XM_011544025.1:c.822T>G	XP_011542327.1:p.Tyr274Ter
XM_011544026.1:c.822T>G	XP_011542328.1:p.Tyr274Ter
XM_011544026.3:c.822T>G	XP_011542328.1:p.Tyr274Ter
XM_011544027.1:c.597T>G	XP_011542329.1:p.Tyr199Ter
XM_011544028.1:c.597T>G	XP_011542330.1:p.Tyr199Ter
XM_011544028.3:c.597T>G	XP_011542330.1:p.Tyr199Ter
XM_011544029.1:c.822T>G	XP_011542331.1:p.Tyr274Ter
XM_017000104.2:c.567T>G	XP_016855593.1:p.Tyr189Ter
XM_017000105.2:c.696T>G	XP_016855594.1:p.Tyr232Ter
XM_024452537.1:c.498T>G	XP_024308305.1:p.Tyr166Ter
XM_024452539.1:c.498T>G	XP_024308307.1:p.Tyr166Ter
XM_024452540.1:c.498T>G	XP_024308308.1:p.Tyr166Ter
XM_024452547.1:c.402T>G	XP_024308315.1:p.Tyr134Ter
XM_024452548.1:c.498T>G	XP_024308316.1:p.Tyr166Ter
XM_024452549.1:c.402T>G	XP_024308317.1:p.Tyr134Ter
XR_002958955.1:n.738T>G
XR_002958956.1:n.738T>G
XR_002958965.1:n.738T>G
XR_949128.1:n.846T>G