Canonical Allele Identifier: CA395345023

Gene: SULT1A1

Linked Data

• MyVariant Identifiers: chr16:g.28631397C>A (hg19) ; chr16:g.28620076C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620076C>A , CM000678.2:g.28620076C>A	GRCh38
NC_000016.9:g.28631397C>A , CM000678.1:g.28631397C>A	GRCh37
NC_000016.8:g.28538898C>A	NCBI36
NG_028128.1:g.8470G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698935.1:n.410G>T
ENST00000395607.6:c.125G>T	ENSP00000378971.2:p.Trp42Leu
ENST00000395609.6:n.483G>T
ENST00000677940.1:c.125G>T	ENSP00000503077.1:p.Trp42Leu
ENST00000679262.1:c.*105G>T	ENSP00000502863.1:n.*105G>T
ENST00000350842.8:c.125G>T	ENSP00000329399.4:p.Trp42Leu
ENST00000395609.5:c.-279G>T	ENSP00000378972.1:n.-279G>T
ENST00000562058.5:c.125G>T	ENSP00000456215.1:p.Trp42Leu
ENST00000563493.1:c.125G>T	ENSP00000457083.1:p.Trp42Leu
ENST00000564818.5:c.125G>T	ENSP00000454388.1:p.Trp42Leu
NM_177536.3:c.125G>T	NP_803880.1:p.Trp42Leu
XM_017023607.2:c.-79G>T	XP_016879096.1:n.-79G>T
XM_017023611.2:c.-279G>T	XP_016879100.1:n.-279G>T
XM_017023612.2:c.-203G>T	XP_016879101.1:n.-203G>T
XM_017023613.2:c.-18G>T	XP_016879102.1:n.-18G>T
XM_024450408.1:c.-79G>T	XP_024306176.1:n.-79G>T
XM_024450409.1:c.-1182G>T	XP_024306177.1:n.-1182G>T
XM_024450410.1:c.-782G>T	XP_024306178.1:n.-782G>T
XM_024450411.1:c.-1075G>T	XP_024306179.1:n.-1075G>T
NM_177536.4:c.125G>T	NP_803880.1:p.Trp42Leu
NM_001394421.1:c.-352G>T	NP_001381350.1:n.-352G>T
NM_001394422.1:c.-1151G>T	NP_001381351.1:n.-1151G>T
NM_001394423.1:c.-482G>T	NP_001381352.1:n.-482G>T
NM_001394424.1:c.-49G>T	NP_001381353.1:n.-49G>T
NM_001394425.1:c.-279G>T	NP_001381354.1:n.-279G>T
NM_177536.5:c.56G>T	NP_803880.2:p.Trp19Leu