Canonical Allele Identifier: CA2038198170

Gene: SUOX

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56005115_56005116delinsTC , CM000674.2:g.56005115_56005116delinsTC	GRCh38
NC_000012.11:g.56398899_56398900delinsTC , CM000674.1:g.56398899_56398900delinsTC	GRCh37
NC_000012.10:g.54685166_54685167delinsTC	NCBI36
NG_008136.1:g.12857_12858delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266971.8:c.*88_*89delinsTC MANE Select	ENSP00000266971.3:n.*88_*89delinsTC
ENST00000266971.7:c.*88_*89delinsTC	ENSP00000266971.3:n.*88_*89delinsTC
ENST00000356124.8:c.*88_*89delinsTC	ENSP00000348440.4:n.*88_*89delinsTC
ENST00000394109.7:c.*88_*89delinsTC	ENSP00000377668.3:n.*88_*89delinsTC
ENST00000394115.6:c.*88_*89delinsTC	ENSP00000377674.2:n.*88_*89delinsTC
ENST00000548274.5:c.*88_*89delinsTC	ENSP00000450245.1:n.*88_*89delinsTC
ENST00000550065.1:c.*88_*89delinsTC	ENSP00000450264.1:n.*88_*89delinsTC
NM_000456.2:c.*88_*89delinsTC	NP_000447.2:n.*88_*89delinsTC
NM_001032386.1:c.*88_*89delinsTC	NP_001027558.1:n.*88_*89delinsTC
NM_001032387.1:c.*88_*89delinsTC	NP_001027559.1:n.*88_*89delinsTC
XM_005269112.1:c.*88_*89delinsTC	XP_005269169.1:n.*88_*89delinsTC
XM_017019905.2:c.*88_*89delinsTC	XP_016875394.1:n.*88_*89delinsTC
XM_017019906.1:c.*88_*89delinsTC	XP_016875395.1:n.*88_*89delinsTC
XM_017019907.2:c.*88_*89delinsTC	XP_016875396.1:n.*88_*89delinsTC
XM_017019908.1:c.*88_*89delinsTC	XP_016875397.1:n.*88_*89delinsTC
XM_024449167.1:c.*88_*89delinsTC	XP_024304935.1:n.*88_*89delinsTC
NM_001032386.2:c.*88_*89delinsTC MANE Select	NP_001027558.1:n.*88_*89delinsTC
NM_000456.3:c.*88_*89delinsTC	NP_000447.2:n.*88_*89delinsTC
NM_001032387.2:c.*88_*89delinsTC	NP_001027559.1:n.*88_*89delinsTC