Canonical Allele Identifier: CA2632511348
Gene: SULT1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28609437T>C , CM000678.2:g.28609437T>C GRCh38
NC_000016.9:g.28620758T>C , CM000678.1:g.28620758T>C GRCh37
NC_000016.8:g.28528259T>C NCBI36
NG_028128.1:g.19109A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000314752.12:c.-5+494A>G MANE Select ENSP00000321988.7:n.-5+494A>G
ENST00000395607.6:c.*722A>G ENSP00000378971.2:n.*722A>G
ENST00000395609.6:n.1251A>G
ENST00000677940.1:c.138+10626A>G ENSP00000503077.1:n.138+10626A>G
ENST00000679262.1:c.*118+10626A>G ENSP00000502863.1:n.*118+10626A>G
ENST00000314752.11:c.-5+494A>G ENSP00000321988.7:n.-5+494A>G
ENST00000350842.8:c.139-2360A>G ENSP00000329399.4:n.139-2360A>G
ENST00000395609.5:c.-5+494A>G ENSP00000378972.1:n.-5+494A>G
ENST00000562058.5:c.*228+494A>G ENSP00000456215.1:n.*228+494A>G
ENST00000563493.1:c.139-578A>G ENSP00000457083.1:n.139-578A>G
ENST00000564818.5:c.*229-2A>G ENSP00000454388.1:n.*229-2A>G
ENST00000566189.5:c.-36+494A>G ENSP00000456459.1:n.-36+494A>G
ENST00000567512.1:c.-5+494A>G ENSP00000455979.1:n.-5+494A>G
ENST00000567998.5:n.4843A>G
NM_001055.3:c.-5+494A>G NP_001046.2:n.-5+494A>G
NM_177529.2:c.-36+494A>G NP_803565.1:n.-36+494A>G
NM_177536.3:c.139-2360A>G NP_803880.1:n.139-2360A>G
XM_017023604.1:c.-79A>G XP_016879093.1:n.-79A>G
XM_017023605.1:c.-77-2A>G XP_016879094.1:n.-77-2A>G
XM_017023607.2:c.197-2A>G XP_016879096.1:n.197-2A>G
XM_017023608.1:c.-5+494A>G XP_016879097.1:n.-5+494A>G
XM_017023611.2:c.-5+494A>G XP_016879100.1:n.-5+494A>G
XM_017023612.2:c.-5+494A>G XP_016879101.1:n.-5+494A>G
XM_017023613.2:c.-4-578A>G XP_016879102.1:n.-4-578A>G
XM_024450408.1:c.198A>G XP_024306176.1:p.Ala66=
XM_024450409.1:c.-414A>G XP_024306177.1:n.-414A>G
XM_024450410.1:c.-582A>G XP_024306178.1:n.-582A>G
XM_024450411.1:c.-383A>G XP_024306179.1:n.-383A>G
XR_001751973.1:n.125A>G
NM_177536.4:c.139-2360A>G NP_803880.1:n.139-2360A>G
NM_001055.4:c.-5+494A>G MANE Select NP_001046.2:n.-5+494A>G
NM_001394421.1:c.-77-2A>G NP_001381350.1:n.-77-2A>G
NM_001394422.1:c.-383A>G NP_001381351.1:n.-383A>G
NM_001394423.1:c.-77-2A>G NP_001381352.1:n.-77-2A>G
NM_001394424.1:c.-35-547A>G NP_001381353.1:n.-35-547A>G
NM_001394425.1:c.-5+494A>G NP_001381354.1:n.-5+494A>G
NM_177529.3:c.-36+494A>G NP_803565.1:n.-36+494A>G
NM_177530.4:c.-383A>G NP_803566.1:n.-383A>G
NM_177534.4:c.-582A>G NP_803878.1:n.-582A>G
NM_177536.5:c.70-2360A>G NP_803880.2:n.70-2360A>G