Canonical Allele Identifier: CA2038197813
Gene: SUOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56004304_56004305delinsTG , CM000674.2:g.56004304_56004305delinsTG GRCh38
NC_000012.11:g.56398088_56398089delinsTG , CM000674.1:g.56398088_56398089delinsTG GRCh37
NC_000012.10:g.54684355_54684356delinsTG NCBI36
NG_008136.1:g.12046_12047delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000266971.8:c.915_916delinsTG MANE Select ENSP00000266971.3:p.Ala305=
ENST00000266971.7:c.915_916delinsTG ENSP00000266971.3:p.Ala305=
ENST00000356124.8:c.915_916delinsTG ENSP00000348440.4:p.Ala305=
ENST00000394109.7:c.915_916delinsTG ENSP00000377668.3:p.Ala305=
ENST00000394115.6:c.915_916delinsTG ENSP00000377674.2:p.Ala305=
ENST00000548274.5:c.915_916delinsTG ENSP00000450245.1:p.Ala305=
ENST00000550065.1:c.915_916delinsTG ENSP00000450264.1:p.Ala305=
ENST00000551841.6:c.*103_*104delinsTG ENSP00000449443.1:n.*103_*104delinsTG
NM_000456.2:c.915_916delinsTG NP_000447.2:p.Ala305=
NM_001032386.1:c.915_916delinsTG NP_001027558.1:p.Ala305=
NM_001032387.1:c.915_916delinsTG NP_001027559.1:p.Ala305=
XM_005269112.1:c.936_937delinsTG XP_005269169.1:p.Ala312=
XM_017019905.2:c.936_937delinsTG XP_016875394.1:p.Ala312=
XM_017019906.1:c.936_937delinsTG XP_016875395.1:p.Ala312=
XM_017019907.2:c.915_916delinsTG XP_016875396.1:p.Ala305=
XM_017019908.1:c.915_916delinsTG XP_016875397.1:p.Ala305=
XM_024449167.1:c.936_937delinsTG XP_024304935.1:p.Ala312=
NM_001032386.2:c.915_916delinsTG MANE Select NP_001027558.1:p.Ala305=
NM_000456.3:c.915_916delinsTG NP_000447.2:p.Ala305=
NM_001032387.2:c.915_916delinsTG NP_001027559.1:p.Ala305=