Canonical Allele Identifier: CA395345033

Gene: SULT1A1

Linked Data

• gnomAD v3: 16-28620080-A-C
• gnomAD v4: 16-28620080-A-C
• MyVariant Identifiers: chr16:g.28631401A>C (hg19) ; chr16:g.28620080A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620080A>C , CM000678.2:g.28620080A>C	GRCh38
NC_000016.9:g.28631401A>C , CM000678.1:g.28631401A>C	GRCh37
NC_000016.8:g.28538902A>C	NCBI36
NG_028128.1:g.8466T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698935.1:n.406T>G
ENST00000395607.6:c.121T>G	ENSP00000378971.2:p.Phe41Val
ENST00000395609.6:n.479T>G
ENST00000677940.1:c.121T>G	ENSP00000503077.1:p.Phe41Val
ENST00000679262.1:c.*101T>G	ENSP00000502863.1:n.*101T>G
ENST00000350842.8:c.121T>G	ENSP00000329399.4:p.Phe41Val
ENST00000395609.5:c.-283T>G	ENSP00000378972.1:n.-283T>G
ENST00000562058.5:c.121T>G	ENSP00000456215.1:p.Phe41Val
ENST00000563493.1:c.121T>G	ENSP00000457083.1:p.Phe41Val
ENST00000564818.5:c.121T>G	ENSP00000454388.1:p.Phe41Val
NM_177536.3:c.121T>G	NP_803880.1:p.Phe41Val
XM_017023607.2:c.-83T>G	XP_016879096.1:n.-83T>G
XM_017023611.2:c.-283T>G	XP_016879100.1:n.-283T>G
XM_017023612.2:c.-207T>G	XP_016879101.1:n.-207T>G
XM_017023613.2:c.-22T>G	XP_016879102.1:n.-22T>G
XM_024450408.1:c.-83T>G	XP_024306176.1:n.-83T>G
XM_024450409.1:c.-1186T>G	XP_024306177.1:n.-1186T>G
XM_024450410.1:c.-786T>G	XP_024306178.1:n.-786T>G
XM_024450411.1:c.-1079T>G	XP_024306179.1:n.-1079T>G
NM_177536.4:c.121T>G	NP_803880.1:p.Phe41Val
NM_001394421.1:c.-356T>G	NP_001381350.1:n.-356T>G
NM_001394422.1:c.-1155T>G	NP_001381351.1:n.-1155T>G
NM_001394423.1:c.-486T>G	NP_001381352.1:n.-486T>G
NM_001394424.1:c.-53T>G	NP_001381353.1:n.-53T>G
NM_001394425.1:c.-283T>G	NP_001381354.1:n.-283T>G
NM_177536.5:c.52T>G	NP_803880.2:p.Phe18Val