Canonical Allele Identifier: CA395361211

Gene: SULT1A1

Linked Data

• MyVariant Identifiers: chr16:g.28617231T>A (hg19) ; chr16:g.28605910T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28605910T>A , CM000678.2:g.28605910T>A	GRCh38
NC_000016.9:g.28617231T>A , CM000678.1:g.28617231T>A	GRCh37
NC_000016.8:g.28524732T>A	NCBI36
NG_028128.1:g.22636A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314752.12:c.799A>T MANE Select	ENSP00000321988.7:p.Thr267Ser
ENST00000395607.6:c.*1451+2798A>T	ENSP00000378971.2:n.*1451+2798A>T
ENST00000395609.6:n.2432A>T
ENST00000677940.1:c.139-12342A>T	ENSP00000503077.1:n.139-12342A>T
ENST00000679262.1:c.*118+14153A>T	ENSP00000502863.1:n.*118+14153A>T
ENST00000314752.11:c.799A>T	ENSP00000321988.7:p.Thr267Ser
ENST00000350842.8:c.565A>T	ENSP00000329399.4:p.Thr189Ser
ENST00000395607.5:c.799A>T	ENSP00000378971.1:p.Thr267Ser
ENST00000395609.5:c.799A>T	ENSP00000378972.1:p.Thr267Ser
ENST00000562058.5:c.*1031A>T	ENSP00000456215.1:n.*1031A>T
ENST00000563493.1:c.*683A>T	ENSP00000457083.1:n.*683A>T
ENST00000564818.5:c.*1104A>T	ENSP00000454388.1:n.*1104A>T
ENST00000566189.5:c.799A>T	ENSP00000456459.1:p.Thr267Ser
ENST00000567998.5:n.7629A>T
ENST00000569554.5:c.799A>T	ENSP00000457912.1:p.Thr267Ser
NM_001055.3:c.799A>T	NP_001046.2:p.Thr267Ser
NM_177529.2:c.799A>T	NP_803565.1:p.Thr267Ser
NM_177530.2:c.799A>T	NP_803566.1:p.Thr267Ser
NM_177534.2:c.799A>T	NP_803878.1:p.Thr267Ser
NM_177536.3:c.565A>T	NP_803880.1:p.Thr189Ser
XM_017023604.1:c.817A>T	XP_016879093.1:p.Thr273Ser
XM_017023605.1:c.817A>T	XP_016879094.1:p.Thr273Ser
XM_017023607.2:c.1072A>T	XP_016879096.1:p.Thr358Ser
XM_017023608.1:c.817A>T	XP_016879097.1:p.Thr273Ser
XM_017023609.1:c.817A>T	XP_016879098.1:p.Thr273Ser
XM_017023610.1:c.817A>T	XP_016879099.1:p.Thr273Ser
XM_017023611.2:c.799A>T	XP_016879100.1:p.Thr267Ser
XM_017023612.2:c.799A>T	XP_016879101.1:p.Thr267Ser
XM_017023613.2:c.799A>T	XP_016879102.1:p.Thr267Ser
XM_024450408.1:c.1075A>T	XP_024306176.1:p.Thr359Ser
XM_024450409.1:c.799A>T	XP_024306177.1:p.Thr267Ser
XM_024450410.1:c.799A>T	XP_024306178.1:p.Thr267Ser
XM_024450411.1:c.799A>T	XP_024306179.1:p.Thr267Ser
XR_001751973.1:n.1040A>T
NM_177530.3:c.799A>T	NP_803566.1:p.Thr267Ser
NM_177534.3:c.799A>T	NP_803878.1:p.Thr267Ser
NM_177536.4:c.565A>T	NP_803880.1:p.Thr189Ser
NM_001055.4:c.799A>T MANE Select	NP_001046.2:p.Thr267Ser
NM_001394421.1:c.799A>T	NP_001381350.1:p.Thr267Ser
NM_001394422.1:c.799A>T	NP_001381351.1:p.Thr267Ser
NM_001394423.1:c.799A>T	NP_001381352.1:p.Thr267Ser
NM_001394424.1:c.799A>T	NP_001381353.1:p.Thr267Ser
NM_001394425.1:c.799A>T	NP_001381354.1:p.Thr267Ser
NM_177529.3:c.799A>T	NP_803565.1:p.Thr267Ser
NM_177530.4:c.799A>T	NP_803566.1:p.Thr267Ser
NM_177534.4:c.799A>T	NP_803878.1:p.Thr267Ser
NM_177536.5:c.496A>T	NP_803880.2:p.Thr166Ser