Canonical Allele Identifier: CA2575962567

Gene: SULT1A1

Linked Data

• gnomAD v4: 16-28620185-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620185T>C , CM000678.2:g.28620185T>C	GRCh38
NC_000016.9:g.28631506T>C , CM000678.1:g.28631506T>C	GRCh37
NC_000016.8:g.28539007T>C	NCBI36
NG_028128.1:g.8361A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698935.1:n.353-52A>G
ENST00000395607.6:c.68-52A>G	ENSP00000378971.2:n.68-52A>G
ENST00000395609.6:n.426-52A>G
ENST00000677940.1:c.68-52A>G	ENSP00000503077.1:n.68-52A>G
ENST00000679262.1:c.*48-52A>G	ENSP00000502863.1:n.*48-52A>G
ENST00000350842.8:c.68-52A>G	ENSP00000329399.4:n.68-52A>G
ENST00000395609.5:c.-336-52A>G	ENSP00000378972.1:n.-336-52A>G
ENST00000562058.5:c.68-52A>G	ENSP00000456215.1:n.68-52A>G
ENST00000563493.1:c.68-52A>G	ENSP00000457083.1:n.68-52A>G
ENST00000564818.5:c.68-52A>G	ENSP00000454388.1:n.68-52A>G
NM_177536.3:c.68-52A>G	NP_803880.1:n.68-52A>G
XM_017023607.2:c.-136-52A>G	XP_016879096.1:n.-136-52A>G
XM_017023611.2:c.-336-52A>G	XP_016879100.1:n.-336-52A>G
XM_017023612.2:c.-260-52A>G	XP_016879101.1:n.-260-52A>G
XM_017023613.2:c.-75-52A>G	XP_016879102.1:n.-75-52A>G
XM_024450408.1:c.-136-52A>G	XP_024306176.1:n.-136-52A>G
XM_024450409.1:c.-1239-52A>G	XP_024306177.1:n.-1239-52A>G
XM_024450410.1:c.-839-52A>G	XP_024306178.1:n.-839-52A>G
XM_024450411.1:c.-1132-52A>G	XP_024306179.1:n.-1132-52A>G
NM_177536.4:c.68-52A>G	NP_803880.1:n.68-52A>G
NM_001394421.1:c.-409-52A>G	NP_001381350.1:n.-409-52A>G
NM_001394422.1:c.-1208-52A>G	NP_001381351.1:n.-1208-52A>G
NM_001394423.1:c.-539-52A>G	NP_001381352.1:n.-539-52A>G
NM_001394424.1:c.-106-52A>G	NP_001381353.1:n.-106-52A>G
NM_001394425.1:c.-336-52A>G	NP_001381354.1:n.-336-52A>G
NM_177536.5:c.-2-52A>G	NP_803880.2:n.-2-52A>G