Canonical Allele Identifier: CA395361147

Gene: SULT1A1

Linked Data

• MyVariant Identifiers: chr16:g.28617215T>A (hg19) ; chr16:g.28605894T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28605894T>A , CM000678.2:g.28605894T>A	GRCh38
NC_000016.9:g.28617215T>A , CM000678.1:g.28617215T>A	GRCh37
NC_000016.8:g.28524716T>A	NCBI36
NG_028128.1:g.22652A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314752.12:c.815A>T MANE Select	ENSP00000321988.7:p.Gln272Leu
ENST00000395607.6:c.*1451+2814A>T	ENSP00000378971.2:n.*1451+2814A>T
ENST00000395609.6:n.2448A>T
ENST00000677940.1:c.139-12326A>T	ENSP00000503077.1:n.139-12326A>T
ENST00000679262.1:c.*118+14169A>T	ENSP00000502863.1:n.*118+14169A>T
ENST00000314752.11:c.815A>T	ENSP00000321988.7:p.Gln272Leu
ENST00000350842.8:c.581A>T	ENSP00000329399.4:p.Gln194Leu
ENST00000395607.5:c.815A>T	ENSP00000378971.1:p.Gln272Leu
ENST00000395609.5:c.815A>T	ENSP00000378972.1:p.Gln272Leu
ENST00000562058.5:c.*1047A>T	ENSP00000456215.1:n.*1047A>T
ENST00000563493.1:c.*699A>T	ENSP00000457083.1:n.*699A>T
ENST00000564818.5:c.*1120A>T	ENSP00000454388.1:n.*1120A>T
ENST00000566189.5:c.815A>T	ENSP00000456459.1:p.Gln272Leu
ENST00000567998.5:n.7645A>T
ENST00000569554.5:c.815A>T	ENSP00000457912.1:p.Gln272Leu
NM_001055.3:c.815A>T	NP_001046.2:p.Gln272Leu
NM_177529.2:c.815A>T	NP_803565.1:p.Gln272Leu
NM_177530.2:c.815A>T	NP_803566.1:p.Gln272Leu
NM_177534.2:c.815A>T	NP_803878.1:p.Gln272Leu
NM_177536.3:c.581A>T	NP_803880.1:p.Gln194Leu
XM_017023604.1:c.833A>T	XP_016879093.1:p.Gln278Leu
XM_017023605.1:c.833A>T	XP_016879094.1:p.Gln278Leu
XM_017023607.2:c.1088A>T	XP_016879096.1:p.Gln363Leu
XM_017023608.1:c.833A>T	XP_016879097.1:p.Gln278Leu
XM_017023609.1:c.833A>T	XP_016879098.1:p.Gln278Leu
XM_017023610.1:c.833A>T	XP_016879099.1:p.Gln278Leu
XM_017023611.2:c.815A>T	XP_016879100.1:p.Gln272Leu
XM_017023612.2:c.815A>T	XP_016879101.1:p.Gln272Leu
XM_017023613.2:c.815A>T	XP_016879102.1:p.Gln272Leu
XM_024450408.1:c.1091A>T	XP_024306176.1:p.Gln364Leu
XM_024450409.1:c.815A>T	XP_024306177.1:p.Gln272Leu
XM_024450410.1:c.815A>T	XP_024306178.1:p.Gln272Leu
XM_024450411.1:c.815A>T	XP_024306179.1:p.Gln272Leu
XR_001751973.1:n.1056A>T
NM_177530.3:c.815A>T	NP_803566.1:p.Gln272Leu
NM_177534.3:c.815A>T	NP_803878.1:p.Gln272Leu
NM_177536.4:c.581A>T	NP_803880.1:p.Gln194Leu
NM_001055.4:c.815A>T MANE Select	NP_001046.2:p.Gln272Leu
NM_001394421.1:c.815A>T	NP_001381350.1:p.Gln272Leu
NM_001394422.1:c.815A>T	NP_001381351.1:p.Gln272Leu
NM_001394423.1:c.815A>T	NP_001381352.1:p.Gln272Leu
NM_001394424.1:c.815A>T	NP_001381353.1:p.Gln272Leu
NM_001394425.1:c.815A>T	NP_001381354.1:p.Gln272Leu
NM_177529.3:c.815A>T	NP_803565.1:p.Gln272Leu
NM_177530.4:c.815A>T	NP_803566.1:p.Gln272Leu
NM_177534.4:c.815A>T	NP_803878.1:p.Gln272Leu
NM_177536.5:c.512A>T	NP_803880.2:p.Gln171Leu