Canonical Allele Identifier: CA797945088
Gene: SULT1E1 HGNC NCBI

Linked Data

dbSNP Id: rs1284616938
MyVariant Identifiers: chr4:g.70724066del (hg19) chr4:g.69858348del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.69858348del , CM000666.2:g.69858348del GRCh38
NC_000004.11:g.70724066del , CM000666.1:g.70724066del GRCh37
NC_000004.10:g.70758655del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000226444.4:c.-9-695del MANE Select ENSP00000226444.3:n.-9-695del
ENST00000226444.3:c.-9-695del ENSP00000226444.3:n.-9-695del
ENST00000504002.1:n.98-695del
NM_005420.2:c.-9-695del NP_005411.1:n.-9-695del
XM_011532209.1:c.-9-695del XP_011530511.1:n.-9-695del
XM_011532210.1:c.-9-695del XP_011530512.1:n.-9-695del
XM_011532210.2:c.-9-695del XP_011530512.1:n.-9-695del
NM_005420.3:c.-9-695del MANE Select NP_005411.1:n.-9-695del
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