Canonical Allele Identifier: CA2038196626

Gene: SUOX

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56001613C= , CM000674.2:g.56001613C=	GRCh38
NC_000012.11:g.56395397C= , CM000674.1:g.56395397C=	GRCh37
NC_000012.10:g.54681664C=	NCBI36
NG_008136.1:g.9355C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000266971.8:c.-10-599C= MANE Select	ENSP00000266971.3:n.-10-599C=
ENST00000266971.7:c.-10-599C=	ENSP00000266971.3:n.-10-599C=
ENST00000356124.8:c.-10-599C=	ENSP00000348440.4:n.-10-599C=
ENST00000394109.7:c.-609C=	ENSP00000377668.3:n.-609C=
ENST00000394115.6:c.-10-599C=	ENSP00000377674.2:n.-10-599C=
ENST00000546833.5:c.-73-273C=	ENSP00000449872.1:n.-73-273C=
ENST00000547586.5:c.-10-599C=	ENSP00000448637.1:n.-10-599C=
ENST00000548274.5:c.-11+141C=	ENSP00000450245.1:n.-11+141C=
ENST00000550121.5:n.449-194C=
ENST00000550340.5:n.54-599C=
ENST00000550478.5:n.131-599C=
ENST00000551698.5:n.191-599C=
ENST00000551841.6:c.-10-599C=	ENSP00000449443.1:n.-10-599C=
ENST00000552258.5:c.-10-599C=	ENSP00000450049.1:n.-10-599C=
ENST00000552363.5:n.82-2005C=
ENST00000552813.5:n.132-599C=
NM_000456.2:c.-10-599C=	NP_000447.2:n.-10-599C=
NM_001032386.1:c.-10-599C=	NP_001027558.1:n.-10-599C=
NM_001032387.1:c.-10-599C=	NP_001027559.1:n.-10-599C=
XM_005269112.1:c.-52-273C=	XP_005269169.1:n.-52-273C=
XM_017019905.2:c.-52-273C=	XP_016875394.1:n.-52-273C=
XM_017019906.1:c.-52-273C=	XP_016875395.1:n.-52-273C=
XM_017019907.2:c.-10-599C=	XP_016875396.1:n.-10-599C=
XM_017019908.1:c.-10-599C=	XP_016875397.1:n.-10-599C=
XM_024449167.1:c.-52-273C=	XP_024304935.1:n.-52-273C=
NM_001032386.2:c.-10-599C= MANE Select	NP_001027558.1:n.-10-599C=
NM_000456.3:c.-10-599C=	NP_000447.2:n.-10-599C=
NM_001032387.2:c.-10-599C=	NP_001027559.1:n.-10-599C=