Canonical Allele Identifier: CA2038197619

Gene: SUOX

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56003854C= , CM000674.2:g.56003854C=	GRCh38
NC_000012.11:g.56397638C= , CM000674.1:g.56397638C=	GRCh37
NC_000012.10:g.54683905C=	NCBI36
NG_008136.1:g.11596C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266971.8:c.465C= MANE Select	ENSP00000266971.3:p.Tyr155=
ENST00000266971.7:c.465C=	ENSP00000266971.3:p.Tyr155=
ENST00000356124.8:c.465C=	ENSP00000348440.4:p.Tyr155=
ENST00000394109.7:c.465C=	ENSP00000377668.3:p.Tyr155=
ENST00000394115.6:c.465C=	ENSP00000377674.2:p.Tyr155=
ENST00000546833.5:c.465C=	ENSP00000449872.1:p.Tyr155=
ENST00000548274.5:c.465C=	ENSP00000450245.1:p.Tyr155=
ENST00000550065.1:c.465C=	ENSP00000450264.1:p.Tyr155=
ENST00000550340.5:n.350C=
ENST00000550478.5:n.544C=
ENST00000551698.5:n.487C=
ENST00000551841.6:c.267+198C=	ENSP00000449443.1:n.267+198C=
NM_000456.2:c.465C=	NP_000447.2:p.Tyr155=
NM_001032386.1:c.465C=	NP_001027558.1:p.Tyr155=
NM_001032387.1:c.465C=	NP_001027559.1:p.Tyr155=
XM_005269112.1:c.486C=	XP_005269169.1:p.Tyr162=
XM_017019905.2:c.486C=	XP_016875394.1:p.Tyr162=
XM_017019906.1:c.486C=	XP_016875395.1:p.Tyr162=
XM_017019907.2:c.465C=	XP_016875396.1:p.Tyr155=
XM_017019908.1:c.465C=	XP_016875397.1:p.Tyr155=
XM_024449167.1:c.486C=	XP_024304935.1:p.Tyr162=
NM_001032386.2:c.465C= MANE Select	NP_001027558.1:p.Tyr155=
NM_000456.3:c.465C=	NP_000447.2:p.Tyr155=
NM_001032387.2:c.465C=	NP_001027559.1:p.Tyr155=