Canonical Allele Identifier: CA385282046

Gene: SUOX

Linked Data

• MyVariant Identifiers: chr12:g.56397439A>C (hg19) ; chr12:g.56003655A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56003655A>C , CM000674.2:g.56003655A>C	GRCh38
NC_000012.11:g.56397439A>C , CM000674.1:g.56397439A>C	GRCh37
NC_000012.10:g.54683706A>C	NCBI36
NG_008136.1:g.11397A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266971.8:c.266A>C MANE Select	ENSP00000266971.3:p.Glu89Ala
ENST00000266971.7:c.266A>C	ENSP00000266971.3:p.Glu89Ala
ENST00000356124.8:c.266A>C	ENSP00000348440.4:p.Glu89Ala
ENST00000394109.7:c.266A>C	ENSP00000377668.3:p.Glu89Ala
ENST00000394115.6:c.266A>C	ENSP00000377674.2:p.Glu89Ala
ENST00000546712.1:n.757A>C
ENST00000546833.5:c.266A>C	ENSP00000449872.1:p.Glu89Ala
ENST00000548274.5:c.266A>C	ENSP00000450245.1:p.Glu89Ala
ENST00000550065.1:c.266A>C	ENSP00000450264.1:p.Glu89Ala
ENST00000550340.5:n.151A>C
ENST00000550478.5:n.345A>C
ENST00000551698.5:n.288A>C
ENST00000551841.6:c.266A>C	ENSP00000449443.1:p.Glu89Ala
ENST00000552258.5:c.266A>C	ENSP00000450049.1:p.Glu89Ala
ENST00000552363.5:n.119A>C
NM_000456.2:c.266A>C	NP_000447.2:p.Glu89Ala
NM_001032386.1:c.266A>C	NP_001027558.1:p.Glu89Ala
NM_001032387.1:c.266A>C	NP_001027559.1:p.Glu89Ala
XM_005269112.1:c.287A>C	XP_005269169.1:p.Glu96Ala
XM_017019905.2:c.287A>C	XP_016875394.1:p.Glu96Ala
XM_017019906.1:c.287A>C	XP_016875395.1:p.Glu96Ala
XM_017019907.2:c.266A>C	XP_016875396.1:p.Glu89Ala
XM_017019908.1:c.266A>C	XP_016875397.1:p.Glu89Ala
XM_024449167.1:c.287A>C	XP_024304935.1:p.Glu96Ala
NM_001032386.2:c.266A>C MANE Select	NP_001027558.1:p.Glu89Ala
NM_000456.3:c.266A>C	NP_000447.2:p.Glu89Ala
NM_001032387.2:c.266A>C	NP_001027559.1:p.Glu89Ala