Canonical Allele Identifier: CA719653486

Gene: SULT1A1

Linked Data

• dbSNP Id: rs1369470701
• MyVariant Identifiers: chr16:g.28631402T>C (hg19) ; chr16:g.28620081T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620081T>C , CM000678.2:g.28620081T>C	GRCh38
NC_000016.9:g.28631402T>C , CM000678.1:g.28631402T>C	GRCh37
NC_000016.8:g.28538903T>C	NCBI36
NG_028128.1:g.8465A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698935.1:n.405A>G
ENST00000395607.6:c.120A>G	ENSP00000378971.2:p.Lys40=
ENST00000395609.6:n.478A>G
ENST00000677940.1:c.120A>G	ENSP00000503077.1:p.Lys40=
ENST00000679262.1:c.*100A>G	ENSP00000502863.1:n.*100A>G
ENST00000350842.8:c.120A>G	ENSP00000329399.4:p.Lys40=
ENST00000395609.5:c.-284A>G	ENSP00000378972.1:n.-284A>G
ENST00000562058.5:c.120A>G	ENSP00000456215.1:p.Lys40=
ENST00000563493.1:c.120A>G	ENSP00000457083.1:p.Lys40=
ENST00000564818.5:c.120A>G	ENSP00000454388.1:p.Lys40=
NM_177536.3:c.120A>G	NP_803880.1:p.Lys40=
XM_017023607.2:c.-84A>G	XP_016879096.1:n.-84A>G
XM_017023611.2:c.-284A>G	XP_016879100.1:n.-284A>G
XM_017023612.2:c.-208A>G	XP_016879101.1:n.-208A>G
XM_017023613.2:c.-23A>G	XP_016879102.1:n.-23A>G
XM_024450408.1:c.-84A>G	XP_024306176.1:n.-84A>G
XM_024450409.1:c.-1187A>G	XP_024306177.1:n.-1187A>G
XM_024450410.1:c.-787A>G	XP_024306178.1:n.-787A>G
XM_024450411.1:c.-1080A>G	XP_024306179.1:n.-1080A>G
NM_177536.4:c.120A>G	NP_803880.1:p.Lys40=
NM_001394421.1:c.-357A>G	NP_001381350.1:n.-357A>G
NM_001394422.1:c.-1156A>G	NP_001381351.1:n.-1156A>G
NM_001394423.1:c.-487A>G	NP_001381352.1:n.-487A>G
NM_001394424.1:c.-54A>G	NP_001381353.1:n.-54A>G
NM_001394425.1:c.-284A>G	NP_001381354.1:n.-284A>G
NM_177536.5:c.51A>G	NP_803880.2:p.Lys17=