Canonical Allele Identifier: CA2174178707

Gene: SQOR

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45642639A= , CM000677.2:g.45642639A=	GRCh38
NC_000015.9:g.45934837A= , CM000677.1:g.45934837A=	GRCh37
NC_000015.8:g.43722129A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260324.12:c.-18+7531A= MANE Select	ENSP00000260324.7:n.-18+7531A=
ENST00000260324.11:c.-18+7531A=	ENSP00000260324.7:n.-18+7531A=
ENST00000561735.5:c.-18+7745A=	ENSP00000456075.1:n.-18+7745A=
ENST00000563296.1:c.-18+10620A=	ENSP00000456979.1:n.-18+10620A=
ENST00000564080.1:c.-17-16268A=	ENSP00000455047.1:n.-17-16268A=
ENST00000565227.1:c.-18+10624A=	ENSP00000457592.1:n.-18+10624A=
ENST00000568606.5:c.-18+10624A=	ENSP00000456019.1:n.-18+10624A=
NM_001271213.1:c.-18+10620A=	NP_001258142.1:n.-18+10620A=
NM_021199.3:c.-18+7531A=	NP_067022.1:n.-18+7531A=
NM_021199.4:c.-18+7531A= MANE Select	NP_067022.1:n.-18+7531A=
NM_001271213.2:c.-18+10620A=	NP_001258142.1:n.-18+10620A=