Canonical Allele Identifier: CA395345010

Gene: SULT1A1

Linked Data

• MyVariant Identifiers: chr16:g.28631392T>C (hg19) ; chr16:g.28620071T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620071T>C , CM000678.2:g.28620071T>C	GRCh38
NC_000016.9:g.28631392T>C , CM000678.1:g.28631392T>C	GRCh37
NC_000016.8:g.28538893T>C	NCBI36
NG_028128.1:g.8475A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698935.1:n.415A>G
ENST00000395607.6:c.130A>G	ENSP00000378971.2:p.Thr44Ala
ENST00000395609.6:n.488A>G
ENST00000677940.1:c.130A>G	ENSP00000503077.1:p.Thr44Ala
ENST00000679262.1:c.*110A>G	ENSP00000502863.1:n.*110A>G
ENST00000350842.8:c.130A>G	ENSP00000329399.4:p.Thr44Ala
ENST00000395609.5:c.-274A>G	ENSP00000378972.1:n.-274A>G
ENST00000562058.5:c.130A>G	ENSP00000456215.1:p.Thr44Ala
ENST00000563493.1:c.130A>G	ENSP00000457083.1:p.Thr44Ala
ENST00000564818.5:c.130A>G	ENSP00000454388.1:p.Thr44Ala
NM_177536.3:c.130A>G	NP_803880.1:p.Thr44Ala
XM_017023607.2:c.-74A>G	XP_016879096.1:n.-74A>G
XM_017023611.2:c.-274A>G	XP_016879100.1:n.-274A>G
XM_017023612.2:c.-198A>G	XP_016879101.1:n.-198A>G
XM_017023613.2:c.-13A>G	XP_016879102.1:n.-13A>G
XM_024450408.1:c.-74A>G	XP_024306176.1:n.-74A>G
XM_024450409.1:c.-1177A>G	XP_024306177.1:n.-1177A>G
XM_024450410.1:c.-777A>G	XP_024306178.1:n.-777A>G
XM_024450411.1:c.-1070A>G	XP_024306179.1:n.-1070A>G
NM_177536.4:c.130A>G	NP_803880.1:p.Thr44Ala
NM_001394421.1:c.-347A>G	NP_001381350.1:n.-347A>G
NM_001394422.1:c.-1146A>G	NP_001381351.1:n.-1146A>G
NM_001394423.1:c.-477A>G	NP_001381352.1:n.-477A>G
NM_001394424.1:c.-44A>G	NP_001381353.1:n.-44A>G
NM_001394425.1:c.-274A>G	NP_001381354.1:n.-274A>G
NM_177536.5:c.61A>G	NP_803880.2:p.Thr21Ala