Canonical Allele Identifier: CA1278105150
Gene: SULT1C4 HGNC NCBI

Linked Data

dbSNP Id: rs1678299349
gnomAD v4: 2-108378377-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378378del , CM000664.2:g.108378378del GRCh38
NC_000002.11:g.108994834del , CM000664.1:g.108994834del GRCh37
NC_000002.10:g.108361266del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.41del MANE Select ENSP00000272452.2:p.Thr14LysfsTer4
ENST00000272452.6:c.41del ENSP00000272452.2:p.Thr14LysfsTer4
ENST00000409309.3:c.41del ENSP00000387225.3:p.Thr14LysfsTer4
ENST00000494122.1:n.468del
NM_006588.2:c.41del NP_006579.2:p.Thr14LysfsTer4
XM_005263919.2:c.41del XP_005263976.1:p.Thr14LysfsTer4
NM_001321770.1:c.41del NP_001308699.1:p.Thr14LysfsTer4
NM_006588.3:c.41del NP_006579.2:p.Thr14LysfsTer4
NR_135776.1:n.468del
NR_135779.1:n.468del
NM_006588.4:c.41del MANE Select NP_006579.2:p.Thr14LysfsTer4
NM_001321770.2:c.41del NP_001308699.1:p.Thr14LysfsTer4
NR_135776.2:n.425del
NR_135779.2:n.425del
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