Canonical Allele Identifier: CA2215753361
Gene: SULT1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28620182G= , CM000678.2:g.28620182G= GRCh38
NC_000016.9:g.28631503G= , CM000678.1:g.28631503G= GRCh37
NC_000016.8:g.28539004G= NCBI36
NG_028128.1:g.8364C=

Transcript Alleles

HGVS Amino-acid change
ENST00000698935.1:n.353-49C=
ENST00000395607.6:c.68-49C= ENSP00000378971.2:n.68-49C=
ENST00000395609.6:n.426-49C=
ENST00000677940.1:c.68-49C= ENSP00000503077.1:n.68-49C=
ENST00000679262.1:c.*48-49C= ENSP00000502863.1:n.*48-49C=
ENST00000350842.8:c.68-49C= ENSP00000329399.4:n.68-49C=
ENST00000395609.5:c.-336-49C= ENSP00000378972.1:n.-336-49C=
ENST00000562058.5:c.68-49C= ENSP00000456215.1:n.68-49C=
ENST00000563493.1:c.68-49C= ENSP00000457083.1:n.68-49C=
ENST00000564818.5:c.68-49C= ENSP00000454388.1:n.68-49C=
NM_177536.3:c.68-49C= NP_803880.1:n.68-49C=
XM_017023607.2:c.-136-49C= XP_016879096.1:n.-136-49C=
XM_017023611.2:c.-336-49C= XP_016879100.1:n.-336-49C=
XM_017023612.2:c.-260-49C= XP_016879101.1:n.-260-49C=
XM_017023613.2:c.-75-49C= XP_016879102.1:n.-75-49C=
XM_024450408.1:c.-136-49C= XP_024306176.1:n.-136-49C=
XM_024450409.1:c.-1239-49C= XP_024306177.1:n.-1239-49C=
XM_024450410.1:c.-839-49C= XP_024306178.1:n.-839-49C=
XM_024450411.1:c.-1132-49C= XP_024306179.1:n.-1132-49C=
NM_177536.4:c.68-49C= NP_803880.1:n.68-49C=
NM_001394421.1:c.-409-49C= NP_001381350.1:n.-409-49C=
NM_001394422.1:c.-1208-49C= NP_001381351.1:n.-1208-49C=
NM_001394423.1:c.-539-49C= NP_001381352.1:n.-539-49C=
NM_001394424.1:c.-106-49C= NP_001381353.1:n.-106-49C=
NM_001394425.1:c.-336-49C= NP_001381354.1:n.-336-49C=
NM_177536.5:c.-2-49C= NP_803880.2:n.-2-49C=