Canonical Allele Identifier: CA395345048

Gene: SULT1A1

Linked Data

• MyVariant Identifiers: chr16:g.28631406T>A (hg19) ; chr16:g.28620085T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620085T>A , CM000678.2:g.28620085T>A	GRCh38
NC_000016.9:g.28631406T>A , CM000678.1:g.28631406T>A	GRCh37
NC_000016.8:g.28538907T>A	NCBI36
NG_028128.1:g.8461A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698935.1:n.401A>T
ENST00000395607.6:c.116A>T	ENSP00000378971.2:p.Gln39Leu
ENST00000395609.6:n.474A>T
ENST00000677940.1:c.116A>T	ENSP00000503077.1:p.Gln39Leu
ENST00000679262.1:c.*96A>T	ENSP00000502863.1:n.*96A>T
ENST00000350842.8:c.116A>T	ENSP00000329399.4:p.Gln39Leu
ENST00000395609.5:c.-288A>T	ENSP00000378972.1:n.-288A>T
ENST00000562058.5:c.116A>T	ENSP00000456215.1:p.Gln39Leu
ENST00000563493.1:c.116A>T	ENSP00000457083.1:p.Gln39Leu
ENST00000564818.5:c.116A>T	ENSP00000454388.1:p.Gln39Leu
NM_177536.3:c.116A>T	NP_803880.1:p.Gln39Leu
XM_017023607.2:c.-88A>T	XP_016879096.1:n.-88A>T
XM_017023611.2:c.-288A>T	XP_016879100.1:n.-288A>T
XM_017023612.2:c.-212A>T	XP_016879101.1:n.-212A>T
XM_017023613.2:c.-27A>T	XP_016879102.1:n.-27A>T
XM_024450408.1:c.-88A>T	XP_024306176.1:n.-88A>T
XM_024450409.1:c.-1191A>T	XP_024306177.1:n.-1191A>T
XM_024450410.1:c.-791A>T	XP_024306178.1:n.-791A>T
XM_024450411.1:c.-1084A>T	XP_024306179.1:n.-1084A>T
NM_177536.4:c.116A>T	NP_803880.1:p.Gln39Leu
NM_001394421.1:c.-361A>T	NP_001381350.1:n.-361A>T
NM_001394422.1:c.-1160A>T	NP_001381351.1:n.-1160A>T
NM_001394423.1:c.-491A>T	NP_001381352.1:n.-491A>T
NM_001394424.1:c.-58A>T	NP_001381353.1:n.-58A>T
NM_001394425.1:c.-288A>T	NP_001381354.1:n.-288A>T
NM_177536.5:c.47A>T	NP_803880.2:p.Gln16Leu