Canonical Allele Identifier: CA2575186018

Gene: SUOX

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56003576A>T , CM000674.2:g.56003576A>T	GRCh38
NC_000012.11:g.56397360A>T , CM000674.1:g.56397360A>T	GRCh37
NC_000012.10:g.54683627A>T	NCBI36
NG_008136.1:g.11318A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266971.8:c.229-42A>T MANE Select	ENSP00000266971.3:n.229-42A>T
ENST00000266971.7:c.229-42A>T	ENSP00000266971.3:n.229-42A>T
ENST00000356124.8:c.229-42A>T	ENSP00000348440.4:n.229-42A>T
ENST00000394109.7:c.229-42A>T	ENSP00000377668.3:n.229-42A>T
ENST00000394115.6:c.229-42A>T	ENSP00000377674.2:n.229-42A>T
ENST00000546712.1:n.720-42A>T
ENST00000546833.5:c.229-42A>T	ENSP00000449872.1:n.229-42A>T
ENST00000548274.5:c.229-42A>T	ENSP00000450245.1:n.229-42A>T
ENST00000550065.1:c.229-42A>T	ENSP00000450264.1:n.229-42A>T
ENST00000550340.5:n.114-42A>T
ENST00000550478.5:n.308-42A>T
ENST00000551698.5:n.251-42A>T
ENST00000551841.6:c.229-42A>T	ENSP00000449443.1:n.229-42A>T
ENST00000552258.5:c.229-42A>T	ENSP00000450049.1:n.229-42A>T
ENST00000552363.5:n.82-42A>T
NM_000456.2:c.229-42A>T	NP_000447.2:n.229-42A>T
NM_001032386.1:c.229-42A>T	NP_001027558.1:n.229-42A>T
NM_001032387.1:c.229-42A>T	NP_001027559.1:n.229-42A>T
XM_005269112.1:c.250-42A>T	XP_005269169.1:n.250-42A>T
XM_017019905.2:c.250-42A>T	XP_016875394.1:n.250-42A>T
XM_017019906.1:c.250-42A>T	XP_016875395.1:n.250-42A>T
XM_017019907.2:c.229-42A>T	XP_016875396.1:n.229-42A>T
XM_017019908.1:c.229-42A>T	XP_016875397.1:n.229-42A>T
XM_024449167.1:c.250-42A>T	XP_024304935.1:n.250-42A>T
NM_001032386.2:c.229-42A>T MANE Select	NP_001027558.1:n.229-42A>T
NM_000456.3:c.229-42A>T	NP_000447.2:n.229-42A>T
NM_001032387.2:c.229-42A>T	NP_001027559.1:n.229-42A>T