Canonical Allele Identifier: CA2804004884

Gene: SQOR

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45642610A>G , CM000677.2:g.45642610A>G	GRCh38
NC_000015.9:g.45934808A>G , CM000677.1:g.45934808A>G	GRCh37
NC_000015.8:g.43722100A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260324.12:c.-18+7502A>G MANE Select	ENSP00000260324.7:n.-18+7502A>G
ENST00000260324.11:c.-18+7502A>G	ENSP00000260324.7:n.-18+7502A>G
ENST00000561735.5:c.-18+7716A>G	ENSP00000456075.1:n.-18+7716A>G
ENST00000563296.1:c.-18+10591A>G	ENSP00000456979.1:n.-18+10591A>G
ENST00000564080.1:c.-17-16297A>G	ENSP00000455047.1:n.-17-16297A>G
ENST00000565227.1:c.-18+10595A>G	ENSP00000457592.1:n.-18+10595A>G
ENST00000568606.5:c.-18+10595A>G	ENSP00000456019.1:n.-18+10595A>G
NM_001271213.1:c.-18+10591A>G	NP_001258142.1:n.-18+10591A>G
NM_021199.3:c.-18+7502A>G	NP_067022.1:n.-18+7502A>G
NM_021199.4:c.-18+7502A>G MANE Select	NP_067022.1:n.-18+7502A>G
NM_001271213.2:c.-18+10591A>G	NP_001258142.1:n.-18+10591A>G