Canonical Allele Identifier: CA395345020

Gene: SULT1A1

Linked Data

• MyVariant Identifiers: chr16:g.28631396C>G (hg19) ; chr16:g.28620075C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620075C>G , CM000678.2:g.28620075C>G	GRCh38
NC_000016.9:g.28631396C>G , CM000678.1:g.28631396C>G	GRCh37
NC_000016.8:g.28538897C>G	NCBI36
NG_028128.1:g.8471G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698935.1:n.411G>C
ENST00000395607.6:c.126G>C	ENSP00000378971.2:p.Trp42Cys
ENST00000395609.6:n.484G>C
ENST00000677940.1:c.126G>C	ENSP00000503077.1:p.Trp42Cys
ENST00000679262.1:c.*106G>C	ENSP00000502863.1:n.*106G>C
ENST00000350842.8:c.126G>C	ENSP00000329399.4:p.Trp42Cys
ENST00000395609.5:c.-278G>C	ENSP00000378972.1:n.-278G>C
ENST00000562058.5:c.126G>C	ENSP00000456215.1:p.Trp42Cys
ENST00000563493.1:c.126G>C	ENSP00000457083.1:p.Trp42Cys
ENST00000564818.5:c.126G>C	ENSP00000454388.1:p.Trp42Cys
NM_177536.3:c.126G>C	NP_803880.1:p.Trp42Cys
XM_017023607.2:c.-78G>C	XP_016879096.1:n.-78G>C
XM_017023611.2:c.-278G>C	XP_016879100.1:n.-278G>C
XM_017023612.2:c.-202G>C	XP_016879101.1:n.-202G>C
XM_017023613.2:c.-17G>C	XP_016879102.1:n.-17G>C
XM_024450408.1:c.-78G>C	XP_024306176.1:n.-78G>C
XM_024450409.1:c.-1181G>C	XP_024306177.1:n.-1181G>C
XM_024450410.1:c.-781G>C	XP_024306178.1:n.-781G>C
XM_024450411.1:c.-1074G>C	XP_024306179.1:n.-1074G>C
NM_177536.4:c.126G>C	NP_803880.1:p.Trp42Cys
NM_001394421.1:c.-351G>C	NP_001381350.1:n.-351G>C
NM_001394422.1:c.-1150G>C	NP_001381351.1:n.-1150G>C
NM_001394423.1:c.-481G>C	NP_001381352.1:n.-481G>C
NM_001394424.1:c.-48G>C	NP_001381353.1:n.-48G>C
NM_001394425.1:c.-278G>C	NP_001381354.1:n.-278G>C
NM_177536.5:c.57G>C	NP_803880.2:p.Trp19Cys