Canonical Allele Identifier: CA719653495
Gene: SULT1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1396655769

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28620084_28620085del , CM000678.2:g.28620084_28620085del GRCh38
NC_000016.9:g.28631405_28631406del , CM000678.1:g.28631405_28631406del GRCh37
NC_000016.8:g.28538906_28538907del NCBI36
NG_028128.1:g.8462_8463del

Transcript Alleles

HGVS Amino-acid change
ENST00000698935.1:n.402_403del
ENST00000395607.6:c.117_118del ENSP00000378971.2:p.Lys40IlefsTer?
ENST00000395609.6:n.475_476del
ENST00000677940.1:c.117_118del ENSP00000503077.1:p.Lys40IlefsTer?
ENST00000679262.1:c.*97_*98del ENSP00000502863.1:n.*97_*98del
ENST00000350842.8:c.117_118del ENSP00000329399.4:p.Lys40IlefsTer?
ENST00000395609.5:c.-287_-286del ENSP00000378972.1:n.-287_-286del
ENST00000562058.5:c.117_118del ENSP00000456215.1:p.Lys40IlefsTer?
ENST00000563493.1:c.117_118del ENSP00000457083.1:p.Lys40IlefsTer11
ENST00000564818.5:c.117_118del ENSP00000454388.1:p.Lys40IlefsTer?
NM_177536.3:c.117_118del NP_803880.1:p.Lys40IlefsTer?
XM_017023607.2:c.-87_-86del XP_016879096.1:n.-87_-86del
XM_017023611.2:c.-287_-286del XP_016879100.1:n.-287_-286del
XM_017023612.2:c.-211_-210del XP_016879101.1:n.-211_-210del
XM_017023613.2:c.-26_-25del XP_016879102.1:n.-26_-25del
XM_024450408.1:c.-87_-86del XP_024306176.1:n.-87_-86del
XM_024450409.1:c.-1190_-1189del XP_024306177.1:n.-1190_-1189del
XM_024450410.1:c.-790_-789del XP_024306178.1:n.-790_-789del
XM_024450411.1:c.-1083_-1082del XP_024306179.1:n.-1083_-1082del
NM_177536.4:c.117_118del NP_803880.1:p.Lys40IlefsTer?
NM_001394421.1:c.-360_-359del NP_001381350.1:n.-360_-359del
NM_001394422.1:c.-1159_-1158del NP_001381351.1:n.-1159_-1158del
NM_001394423.1:c.-490_-489del NP_001381352.1:n.-490_-489del
NM_001394424.1:c.-57_-56del NP_001381353.1:n.-57_-56del
NM_001394425.1:c.-287_-286del NP_001381354.1:n.-287_-286del
NM_177536.5:c.48_49del NP_803880.2:p.Lys17IlefsTer?