Canonical Allele Identifier: CA2038197810

Gene: SUOX

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56004296_56004297delinsGC , CM000674.2:g.56004296_56004297delinsGC	GRCh38
NC_000012.11:g.56398080_56398081delinsGC , CM000674.1:g.56398080_56398081delinsGC	GRCh37
NC_000012.10:g.54684347_54684348delinsGC	NCBI36
NG_008136.1:g.12038_12039delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266971.8:c.907_908delinsGC MANE Select	ENSP00000266971.3:p.Ala303=
ENST00000266971.7:c.907_908delinsGC	ENSP00000266971.3:p.Ala303=
ENST00000356124.8:c.907_908delinsGC	ENSP00000348440.4:p.Ala303=
ENST00000394109.7:c.907_908delinsGC	ENSP00000377668.3:p.Ala303=
ENST00000394115.6:c.907_908delinsGC	ENSP00000377674.2:p.Ala303=
ENST00000548274.5:c.907_908delinsGC	ENSP00000450245.1:p.Ala303=
ENST00000550065.1:c.907_908delinsGC	ENSP00000450264.1:p.Ala303=
ENST00000551841.6:c.*95_*96delinsGC	ENSP00000449443.1:n.*95_*96delinsGC
NM_000456.2:c.907_908delinsGC	NP_000447.2:p.Ala303=
NM_001032386.1:c.907_908delinsGC	NP_001027558.1:p.Ala303=
NM_001032387.1:c.907_908delinsGC	NP_001027559.1:p.Ala303=
XM_005269112.1:c.928_929delinsGC	XP_005269169.1:p.Ala310=
XM_017019905.2:c.928_929delinsGC	XP_016875394.1:p.Ala310=
XM_017019906.1:c.928_929delinsGC	XP_016875395.1:p.Ala310=
XM_017019907.2:c.907_908delinsGC	XP_016875396.1:p.Ala303=
XM_017019908.1:c.907_908delinsGC	XP_016875397.1:p.Ala303=
XM_024449167.1:c.928_929delinsGC	XP_024304935.1:p.Ala310=
NM_001032386.2:c.907_908delinsGC MANE Select	NP_001027558.1:p.Ala303=
NM_000456.3:c.907_908delinsGC	NP_000447.2:p.Ala303=
NM_001032387.2:c.907_908delinsGC	NP_001027559.1:p.Ala303=