Canonical Allele Identifier: CA395345029

Gene: SULT1A1

Linked Data

• MyVariant Identifiers: chr16:g.28631399G>T (hg19) ; chr16:g.28620078G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620078G>T , CM000678.2:g.28620078G>T	GRCh38
NC_000016.9:g.28631399G>T , CM000678.1:g.28631399G>T	GRCh37
NC_000016.8:g.28538900G>T	NCBI36
NG_028128.1:g.8468C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698935.1:n.408C>A
ENST00000395607.6:c.123C>A	ENSP00000378971.2:p.Phe41Leu
ENST00000395609.6:n.481C>A
ENST00000677940.1:c.123C>A	ENSP00000503077.1:p.Phe41Leu
ENST00000679262.1:c.*103C>A	ENSP00000502863.1:n.*103C>A
ENST00000350842.8:c.123C>A	ENSP00000329399.4:p.Phe41Leu
ENST00000395609.5:c.-281C>A	ENSP00000378972.1:n.-281C>A
ENST00000562058.5:c.123C>A	ENSP00000456215.1:p.Phe41Leu
ENST00000563493.1:c.123C>A	ENSP00000457083.1:p.Phe41Leu
ENST00000564818.5:c.123C>A	ENSP00000454388.1:p.Phe41Leu
NM_177536.3:c.123C>A	NP_803880.1:p.Phe41Leu
XM_017023607.2:c.-81C>A	XP_016879096.1:n.-81C>A
XM_017023611.2:c.-281C>A	XP_016879100.1:n.-281C>A
XM_017023612.2:c.-205C>A	XP_016879101.1:n.-205C>A
XM_017023613.2:c.-20C>A	XP_016879102.1:n.-20C>A
XM_024450408.1:c.-81C>A	XP_024306176.1:n.-81C>A
XM_024450409.1:c.-1184C>A	XP_024306177.1:n.-1184C>A
XM_024450410.1:c.-784C>A	XP_024306178.1:n.-784C>A
XM_024450411.1:c.-1077C>A	XP_024306179.1:n.-1077C>A
NM_177536.4:c.123C>A	NP_803880.1:p.Phe41Leu
NM_001394421.1:c.-354C>A	NP_001381350.1:n.-354C>A
NM_001394422.1:c.-1153C>A	NP_001381351.1:n.-1153C>A
NM_001394423.1:c.-484C>A	NP_001381352.1:n.-484C>A
NM_001394424.1:c.-51C>A	NP_001381353.1:n.-51C>A
NM_001394425.1:c.-281C>A	NP_001381354.1:n.-281C>A
NM_177536.5:c.54C>A	NP_803880.2:p.Phe18Leu