Canonical Allele Identifier: CA395345045

Gene: SULT1A1

Linked Data

• MyVariant Identifiers: chr16:g.28631405C>G (hg19) ; chr16:g.28620084C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620084C>G , CM000678.2:g.28620084C>G	GRCh38
NC_000016.9:g.28631405C>G , CM000678.1:g.28631405C>G	GRCh37
NC_000016.8:g.28538906C>G	NCBI36
NG_028128.1:g.8462G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698935.1:n.402G>C
ENST00000395607.6:c.117G>C	ENSP00000378971.2:p.Gln39His
ENST00000395609.6:n.475G>C
ENST00000677940.1:c.117G>C	ENSP00000503077.1:p.Gln39His
ENST00000679262.1:c.*97G>C	ENSP00000502863.1:n.*97G>C
ENST00000350842.8:c.117G>C	ENSP00000329399.4:p.Gln39His
ENST00000395609.5:c.-287G>C	ENSP00000378972.1:n.-287G>C
ENST00000562058.5:c.117G>C	ENSP00000456215.1:p.Gln39His
ENST00000563493.1:c.117G>C	ENSP00000457083.1:p.Gln39His
ENST00000564818.5:c.117G>C	ENSP00000454388.1:p.Gln39His
NM_177536.3:c.117G>C	NP_803880.1:p.Gln39His
XM_017023607.2:c.-87G>C	XP_016879096.1:n.-87G>C
XM_017023611.2:c.-287G>C	XP_016879100.1:n.-287G>C
XM_017023612.2:c.-211G>C	XP_016879101.1:n.-211G>C
XM_017023613.2:c.-26G>C	XP_016879102.1:n.-26G>C
XM_024450408.1:c.-87G>C	XP_024306176.1:n.-87G>C
XM_024450409.1:c.-1190G>C	XP_024306177.1:n.-1190G>C
XM_024450410.1:c.-790G>C	XP_024306178.1:n.-790G>C
XM_024450411.1:c.-1083G>C	XP_024306179.1:n.-1083G>C
NM_177536.4:c.117G>C	NP_803880.1:p.Gln39His
NM_001394421.1:c.-360G>C	NP_001381350.1:n.-360G>C
NM_001394422.1:c.-1159G>C	NP_001381351.1:n.-1159G>C
NM_001394423.1:c.-490G>C	NP_001381352.1:n.-490G>C
NM_001394424.1:c.-57G>C	NP_001381353.1:n.-57G>C
NM_001394425.1:c.-287G>C	NP_001381354.1:n.-287G>C
NM_177536.5:c.48G>C	NP_803880.2:p.Gln16His