Canonical Allele Identifier: CA2215753438
Community Standard Title: NM_001055.4(SULT1A1):c.-4-392G=
Gene: SULT1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28609251C= , CM000678.2:g.28609251C= GRCh38
NC_000016.9:g.28620572C= , CM000678.1:g.28620572C= GRCh37
NC_000016.8:g.28528073C= NCBI36
NG_028128.1:g.19295G=

Transcript Alleles

HGVS Amino-acid Change
NM_001055.4:c.-4-392G= MANE Select NP_001046.2:n.-4-392G=
ENST00000314752.12:c.-4-392G= MANE Select ENSP00000321988.7:n.-4-392G=
NM_001055.3:c.-4-392G= NP_001046.2:n.-4-392G=
NM_001394421.1:c.-5+112G= NP_001381350.1:n.-5+112G=
NM_001394422.1:c.-197G= NP_001381351.1:n.-197G=
NM_001394423.1:c.-5+112G= NP_001381352.1:n.-5+112G=
NM_001394424.1:c.-35-361G= NP_001381353.1:n.-35-361G=
NM_001394425.1:c.-4-392G= NP_001381354.1:n.-4-392G=
NM_177529.2:c.-35-361G= NP_803565.1:n.-35-361G=
NM_177529.3:c.-35-361G= NP_803565.1:n.-35-361G=
NM_177530.2:c.-197G= NP_803566.1:n.-197G=
NM_177530.3:c.-197G= NP_803566.1:n.-197G=
NM_177530.4:c.-197G= NP_803566.1:n.-197G=
NM_177534.2:c.-396G= NP_803878.1:n.-396G=
NM_177534.3:c.-396G= NP_803878.1:n.-396G=
NM_177534.4:c.-396G= NP_803878.1:n.-396G=
NM_177536.3:c.139-2174G= NP_803880.1:n.139-2174G=
NM_177536.4:c.139-2174G= NP_803880.1:n.139-2174G=
NM_177536.5:c.70-2174G= NP_803880.2:n.70-2174G=
ENST00000314752.11:c.-4-392G= ENSP00000321988.7:n.-4-392G=
ENST00000350842.8:c.139-2174G= ENSP00000329399.4:n.139-2174G=
ENST00000395607.5:c.-197G= ENSP00000378971.1:n.-197G=
ENST00000395607.6:c.*908G= ENSP00000378971.2:n.*908G=
ENST00000395609.5:c.-4-392G= ENSP00000378972.1:n.-4-392G=
ENST00000395609.6:n.1437G=
ENST00000562058.5:c.*229-392G= ENSP00000456215.1:n.*229-392G=
ENST00000563493.1:c.139-392G= ENSP00000457083.1:n.139-392G=
ENST00000564818.5:c.*301+112G= ENSP00000454388.1:n.*301+112G=
ENST00000566189.5:c.-35-361G= ENSP00000456459.1:n.-35-361G=
ENST00000567512.1:c.-4-392G= ENSP00000455979.1:n.-4-392G=
ENST00000567998.5:n.5029G=
ENST00000677940.1:c.138+10812G= ENSP00000503077.1:n.138+10812G=
ENST00000679262.1:c.*118+10812G= ENSP00000502863.1:n.*118+10812G=
XM_017023604.1:c.-5+112G= XP_016879093.1:n.-5+112G=
XM_017023605.1:c.-5+112G= XP_016879094.1:n.-5+112G=
XM_017023607.2:c.269+112G= XP_016879096.1:n.269+112G=
XM_017023608.1:c.-4-392G= XP_016879097.1:n.-4-392G=
XM_017023611.2:c.-4-392G= XP_016879100.1:n.-4-392G=
XM_017023612.2:c.-4-392G= XP_016879101.1:n.-4-392G=
XM_017023613.2:c.-4-392G= XP_016879102.1:n.-4-392G=
XM_024450408.1:c.272+112G= XP_024306176.1:n.272+112G=
XM_024450409.1:c.-228G= XP_024306177.1:n.-228G=
XM_024450410.1:c.-396G= XP_024306178.1:n.-396G=
XM_024450411.1:c.-197G= XP_024306179.1:n.-197G=
XR_001751973.1:n.199+112G=