Canonical Allele Identifier: CA2215718704
Gene: SULT1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28605933C= , CM000678.2:g.28605933C= GRCh38
NC_000016.9:g.28617254C= , CM000678.1:g.28617254C= GRCh37
NC_000016.8:g.28524755C= NCBI36
NG_028128.1:g.22613G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314752.12:c.776G= MANE Select ENSP00000321988.7:p.Gly259=
ENST00000395607.6:c.*1451+2775G= ENSP00000378971.2:n.*1451+2775G=
ENST00000395609.6:n.2409G=
ENST00000677940.1:c.139-12365G= ENSP00000503077.1:n.139-12365G=
ENST00000679262.1:c.*118+14130G= ENSP00000502863.1:n.*118+14130G=
ENST00000314752.11:c.776G= ENSP00000321988.7:p.Gly259=
ENST00000350842.8:c.542G= ENSP00000329399.4:p.Gly181=
ENST00000395607.5:c.776G= ENSP00000378971.1:p.Gly259=
ENST00000395609.5:c.776G= ENSP00000378972.1:p.Gly259=
ENST00000562058.5:c.*1008G= ENSP00000456215.1:n.*1008G=
ENST00000563493.1:c.*660G= ENSP00000457083.1:n.*660G=
ENST00000564818.5:c.*1081G= ENSP00000454388.1:n.*1081G=
ENST00000566189.5:c.776G= ENSP00000456459.1:p.Gly259=
ENST00000567998.5:n.7606G=
ENST00000569554.5:c.776G= ENSP00000457912.1:p.Gly259=
NM_001055.3:c.776G= NP_001046.2:p.Gly259=
NM_177529.2:c.776G= NP_803565.1:p.Gly259=
NM_177530.2:c.776G= NP_803566.1:p.Gly259=
NM_177534.2:c.776G= NP_803878.1:p.Gly259=
NM_177536.3:c.542G= NP_803880.1:p.Gly181=
XM_017023604.1:c.794G= XP_016879093.1:p.Gly265=
XM_017023605.1:c.794G= XP_016879094.1:p.Gly265=
XM_017023607.2:c.1049G= XP_016879096.1:p.Gly350=
XM_017023608.1:c.794G= XP_016879097.1:p.Gly265=
XM_017023609.1:c.794G= XP_016879098.1:p.Gly265=
XM_017023610.1:c.794G= XP_016879099.1:p.Gly265=
XM_017023611.2:c.776G= XP_016879100.1:p.Gly259=
XM_017023612.2:c.776G= XP_016879101.1:p.Gly259=
XM_017023613.2:c.776G= XP_016879102.1:p.Gly259=
XM_024450408.1:c.1052G= XP_024306176.1:p.Gly351=
XM_024450409.1:c.776G= XP_024306177.1:p.Gly259=
XM_024450410.1:c.776G= XP_024306178.1:p.Gly259=
XM_024450411.1:c.776G= XP_024306179.1:p.Gly259=
XR_001751973.1:n.1017G=
NM_177530.3:c.776G= NP_803566.1:p.Gly259=
NM_177534.3:c.776G= NP_803878.1:p.Gly259=
NM_177536.4:c.542G= NP_803880.1:p.Gly181=
NM_001055.4:c.776G= MANE Select NP_001046.2:p.Gly259=
NM_001394421.1:c.776G= NP_001381350.1:p.Gly259=
NM_001394422.1:c.776G= NP_001381351.1:p.Gly259=
NM_001394423.1:c.776G= NP_001381352.1:p.Gly259=
NM_001394424.1:c.776G= NP_001381353.1:p.Gly259=
NM_001394425.1:c.776G= NP_001381354.1:p.Gly259=
NM_177529.3:c.776G= NP_803565.1:p.Gly259=
NM_177530.4:c.776G= NP_803566.1:p.Gly259=
NM_177534.4:c.776G= NP_803878.1:p.Gly259=
NM_177536.5:c.473G= NP_803880.2:p.Gly158=