Canonical Allele Identifier: CA395345014

Gene: SULT1A1

Linked Data

• MyVariant Identifiers: chr16:g.28631394T>C (hg19) ; chr16:g.28620073T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620073T>C , CM000678.2:g.28620073T>C	GRCh38
NC_000016.9:g.28631394T>C , CM000678.1:g.28631394T>C	GRCh37
NC_000016.8:g.28538895T>C	NCBI36
NG_028128.1:g.8473A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698935.1:n.413A>G
ENST00000395607.6:c.128A>G	ENSP00000378971.2:p.Asn43Ser
ENST00000395609.6:n.486A>G
ENST00000677940.1:c.128A>G	ENSP00000503077.1:p.Asn43Ser
ENST00000679262.1:c.*108A>G	ENSP00000502863.1:n.*108A>G
ENST00000350842.8:c.128A>G	ENSP00000329399.4:p.Asn43Ser
ENST00000395609.5:c.-276A>G	ENSP00000378972.1:n.-276A>G
ENST00000562058.5:c.128A>G	ENSP00000456215.1:p.Asn43Ser
ENST00000563493.1:c.128A>G	ENSP00000457083.1:p.Asn43Ser
ENST00000564818.5:c.128A>G	ENSP00000454388.1:p.Asn43Ser
NM_177536.3:c.128A>G	NP_803880.1:p.Asn43Ser
XM_017023607.2:c.-76A>G	XP_016879096.1:n.-76A>G
XM_017023611.2:c.-276A>G	XP_016879100.1:n.-276A>G
XM_017023612.2:c.-200A>G	XP_016879101.1:n.-200A>G
XM_017023613.2:c.-15A>G	XP_016879102.1:n.-15A>G
XM_024450408.1:c.-76A>G	XP_024306176.1:n.-76A>G
XM_024450409.1:c.-1179A>G	XP_024306177.1:n.-1179A>G
XM_024450410.1:c.-779A>G	XP_024306178.1:n.-779A>G
XM_024450411.1:c.-1072A>G	XP_024306179.1:n.-1072A>G
NM_177536.4:c.128A>G	NP_803880.1:p.Asn43Ser
NM_001394421.1:c.-349A>G	NP_001381350.1:n.-349A>G
NM_001394422.1:c.-1148A>G	NP_001381351.1:n.-1148A>G
NM_001394423.1:c.-479A>G	NP_001381352.1:n.-479A>G
NM_001394424.1:c.-46A>G	NP_001381353.1:n.-46A>G
NM_001394425.1:c.-276A>G	NP_001381354.1:n.-276A>G
NM_177536.5:c.59A>G	NP_803880.2:p.Asn20Ser