Canonical Allele Identifier: CA2534674172

Gene: SULT1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620076del , CM000678.2:g.28620076del	GRCh38
NC_000016.9:g.28631397del , CM000678.1:g.28631397del	GRCh37
NC_000016.8:g.28538898del	NCBI36
NG_028128.1:g.8471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698935.1:n.411del
ENST00000395607.6:c.126del	ENSP00000378971.2:p.Trp42Ter
ENST00000395609.6:n.484del
ENST00000677940.1:c.126del	ENSP00000503077.1:p.Trp42Ter
ENST00000679262.1:c.*106del	ENSP00000502863.1:n.*106del
ENST00000350842.8:c.126del	ENSP00000329399.4:p.Trp42Ter
ENST00000395609.5:c.-278del	ENSP00000378972.1:n.-278del
ENST00000562058.5:c.126del	ENSP00000456215.1:p.Trp42Ter
ENST00000563493.1:c.126del	ENSP00000457083.1:p.Trp42Ter
ENST00000564818.5:c.126del	ENSP00000454388.1:p.Trp42Ter
NM_177536.3:c.126del	NP_803880.1:p.Trp42Ter
XM_017023607.2:c.-78del	XP_016879096.1:n.-78del
XM_017023611.2:c.-278del	XP_016879100.1:n.-278del
XM_017023612.2:c.-202del	XP_016879101.1:n.-202del
XM_017023613.2:c.-17del	XP_016879102.1:n.-17del
XM_024450408.1:c.-78del	XP_024306176.1:n.-78del
XM_024450409.1:c.-1181del	XP_024306177.1:n.-1181del
XM_024450410.1:c.-781del	XP_024306178.1:n.-781del
XM_024450411.1:c.-1074del	XP_024306179.1:n.-1074del
NM_177536.4:c.126del	NP_803880.1:p.Trp42Ter
NM_001394421.1:c.-351del	NP_001381350.1:n.-351del
NM_001394422.1:c.-1150del	NP_001381351.1:n.-1150del
NM_001394423.1:c.-481del	NP_001381352.1:n.-481del
NM_001394424.1:c.-48del	NP_001381353.1:n.-48del
NM_001394425.1:c.-278del	NP_001381354.1:n.-278del
NM_177536.5:c.57del	NP_803880.2:p.Trp19Ter