Canonical Allele Identifier: CA2038196631

Gene: SUOX

Linked Data

• dbSNP Id: rs1890532999
• gnomAD v4: 12-56001617-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56001617G>A , CM000674.2:g.56001617G>A	GRCh38
NC_000012.11:g.56395401G>A , CM000674.1:g.56395401G>A	GRCh37
NC_000012.10:g.54681668G>A	NCBI36
NG_008136.1:g.9359G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266971.8:c.-10-595G>A MANE Select	ENSP00000266971.3:n.-10-595G>A
ENST00000266971.7:c.-10-595G>A	ENSP00000266971.3:n.-10-595G>A
ENST00000356124.8:c.-10-595G>A	ENSP00000348440.4:n.-10-595G>A
ENST00000394109.7:c.-605G>A	ENSP00000377668.3:n.-605G>A
ENST00000394115.6:c.-10-595G>A	ENSP00000377674.2:n.-10-595G>A
ENST00000546833.5:c.-73-269G>A	ENSP00000449872.1:n.-73-269G>A
ENST00000547586.5:c.-10-595G>A	ENSP00000448637.1:n.-10-595G>A
ENST00000548274.5:c.-11+145G>A	ENSP00000450245.1:n.-11+145G>A
ENST00000550121.5:n.449-190G>A
ENST00000550340.5:n.54-595G>A
ENST00000550478.5:n.131-595G>A
ENST00000551698.5:n.191-595G>A
ENST00000551841.6:c.-10-595G>A	ENSP00000449443.1:n.-10-595G>A
ENST00000552258.5:c.-10-595G>A	ENSP00000450049.1:n.-10-595G>A
ENST00000552363.5:n.82-2001G>A
ENST00000552813.5:n.132-595G>A
NM_000456.2:c.-10-595G>A	NP_000447.2:n.-10-595G>A
NM_001032386.1:c.-10-595G>A	NP_001027558.1:n.-10-595G>A
NM_001032387.1:c.-10-595G>A	NP_001027559.1:n.-10-595G>A
XM_005269112.1:c.-52-269G>A	XP_005269169.1:n.-52-269G>A
XM_017019905.2:c.-52-269G>A	XP_016875394.1:n.-52-269G>A
XM_017019906.1:c.-52-269G>A	XP_016875395.1:n.-52-269G>A
XM_017019907.2:c.-10-595G>A	XP_016875396.1:n.-10-595G>A
XM_017019908.1:c.-10-595G>A	XP_016875397.1:n.-10-595G>A
XM_024449167.1:c.-52-269G>A	XP_024304935.1:n.-52-269G>A
NM_001032386.2:c.-10-595G>A MANE Select	NP_001027558.1:n.-10-595G>A
NM_000456.3:c.-10-595G>A	NP_000447.2:n.-10-595G>A
NM_001032387.2:c.-10-595G>A	NP_001027559.1:n.-10-595G>A