Canonical Allele Identifier: CA385288222

Gene: SUOX

Linked Data

• MyVariant Identifiers: chr12:g.56398000A>C (hg19) ; chr12:g.56004216A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56004216A>C , CM000674.2:g.56004216A>C	GRCh38
NC_000012.11:g.56398000A>C , CM000674.1:g.56398000A>C	GRCh37
NC_000012.10:g.54684267A>C	NCBI36
NG_008136.1:g.11958A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266971.8:c.827A>C MANE Select	ENSP00000266971.3:p.Lys276Thr
ENST00000266971.7:c.827A>C	ENSP00000266971.3:p.Lys276Thr
ENST00000356124.8:c.827A>C	ENSP00000348440.4:p.Lys276Thr
ENST00000394109.7:c.827A>C	ENSP00000377668.3:p.Lys276Thr
ENST00000394115.6:c.827A>C	ENSP00000377674.2:p.Lys276Thr
ENST00000548274.5:c.827A>C	ENSP00000450245.1:p.Lys276Thr
ENST00000550065.1:c.827A>C	ENSP00000450264.1:p.Lys276Thr
ENST00000551841.6:c.*15A>C	ENSP00000449443.1:n.*15A>C
NM_000456.2:c.827A>C	NP_000447.2:p.Lys276Thr
NM_001032386.1:c.827A>C	NP_001027558.1:p.Lys276Thr
NM_001032387.1:c.827A>C	NP_001027559.1:p.Lys276Thr
XM_005269112.1:c.848A>C	XP_005269169.1:p.Lys283Thr
XM_017019905.2:c.848A>C	XP_016875394.1:p.Lys283Thr
XM_017019906.1:c.848A>C	XP_016875395.1:p.Lys283Thr
XM_017019907.2:c.827A>C	XP_016875396.1:p.Lys276Thr
XM_017019908.1:c.827A>C	XP_016875397.1:p.Lys276Thr
XM_024449167.1:c.848A>C	XP_024304935.1:p.Lys283Thr
NM_001032386.2:c.827A>C MANE Select	NP_001027558.1:p.Lys276Thr
NM_000456.3:c.827A>C	NP_000447.2:p.Lys276Thr
NM_001032387.2:c.827A>C	NP_001027559.1:p.Lys276Thr