Canonical Allele Identifier: CA621716973

Gene: SULT1A1

Linked Data

• dbSNP Id: rs1452231617
• gnomAD v2: 16-28620788-T-C
• gnomAD v4: 16-28609467-T-C
• MyVariant Identifiers: chr16:g.28620788T>C (hg19) ; chr16:g.28609467T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28609467T>C , CM000678.2:g.28609467T>C	GRCh38
NC_000016.9:g.28620788T>C , CM000678.1:g.28620788T>C	GRCh37
NC_000016.8:g.28528289T>C	NCBI36
NG_028128.1:g.19079A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314752.12:c.-5+464A>G MANE Select	ENSP00000321988.7:n.-5+464A>G
ENST00000395607.6:c.*692A>G	ENSP00000378971.2:n.*692A>G
ENST00000395609.6:n.1221A>G
ENST00000677940.1:c.138+10596A>G	ENSP00000503077.1:n.138+10596A>G
ENST00000679262.1:c.*118+10596A>G	ENSP00000502863.1:n.*118+10596A>G
ENST00000314752.11:c.-5+464A>G	ENSP00000321988.7:n.-5+464A>G
ENST00000350842.8:c.139-2390A>G	ENSP00000329399.4:n.139-2390A>G
ENST00000395609.5:c.-5+464A>G	ENSP00000378972.1:n.-5+464A>G
ENST00000562058.5:c.*228+464A>G	ENSP00000456215.1:n.*228+464A>G
ENST00000563493.1:c.139-608A>G	ENSP00000457083.1:n.139-608A>G
ENST00000564818.5:c.*229-32A>G	ENSP00000454388.1:n.*229-32A>G
ENST00000566189.5:c.-36+464A>G	ENSP00000456459.1:n.-36+464A>G
ENST00000567512.1:c.-5+464A>G	ENSP00000455979.1:n.-5+464A>G
ENST00000567998.5:n.4813A>G
NM_001055.3:c.-5+464A>G	NP_001046.2:n.-5+464A>G
NM_177529.2:c.-36+464A>G	NP_803565.1:n.-36+464A>G
NM_177536.3:c.139-2390A>G	NP_803880.1:n.139-2390A>G
XM_017023604.1:c.-80-29A>G	XP_016879093.1:n.-80-29A>G
XM_017023605.1:c.-77-32A>G	XP_016879094.1:n.-77-32A>G
XM_017023607.2:c.197-32A>G	XP_016879096.1:n.197-32A>G
XM_017023608.1:c.-5+464A>G	XP_016879097.1:n.-5+464A>G
XM_017023611.2:c.-5+464A>G	XP_016879100.1:n.-5+464A>G
XM_017023612.2:c.-5+464A>G	XP_016879101.1:n.-5+464A>G
XM_017023613.2:c.-4-608A>G	XP_016879102.1:n.-4-608A>G
XM_024450408.1:c.197-29A>G	XP_024306176.1:n.197-29A>G
XM_024450409.1:c.-444A>G	XP_024306177.1:n.-444A>G
XM_024450410.1:c.-583-29A>G	XP_024306178.1:n.-583-29A>G
XM_024450411.1:c.-413A>G	XP_024306179.1:n.-413A>G
XR_001751973.1:n.124-29A>G
NM_177536.4:c.139-2390A>G	NP_803880.1:n.139-2390A>G
NM_001055.4:c.-5+464A>G MANE Select	NP_001046.2:n.-5+464A>G
NM_001394421.1:c.-77-32A>G	NP_001381350.1:n.-77-32A>G
NM_001394422.1:c.-413A>G	NP_001381351.1:n.-413A>G
NM_001394423.1:c.-77-32A>G	NP_001381352.1:n.-77-32A>G
NM_001394424.1:c.-35-577A>G	NP_001381353.1:n.-35-577A>G
NM_001394425.1:c.-5+464A>G	NP_001381354.1:n.-5+464A>G
NM_177529.3:c.-36+464A>G	NP_803565.1:n.-36+464A>G
NM_177530.4:c.-413A>G	NP_803566.1:n.-413A>G
NM_177534.4:c.-612A>G	NP_803878.1:n.-612A>G
NM_177536.5:c.70-2390A>G	NP_803880.2:n.70-2390A>G