Canonical Allele Identifier: CA1278105185
Gene: SULT1C4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378467A= , CM000664.2:g.108378467A= GRCh38
NC_000002.11:g.108994923A= , CM000664.1:g.108994923A= GRCh37
NC_000002.10:g.108361355A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.130A= MANE Select ENSP00000272452.2:p.Lys44=
ENST00000272452.6:c.130A= ENSP00000272452.2:p.Lys44=
ENST00000409309.3:c.130A= ENSP00000387225.3:p.Lys44=
ENST00000494122.1:n.557A=
NM_006588.2:c.130A= NP_006579.2:p.Lys44=
XM_005263919.2:c.130A= XP_005263976.1:p.Lys44=
NM_001321770.1:c.130A= NP_001308699.1:p.Lys44=
NM_006588.3:c.130A= NP_006579.2:p.Lys44=
NR_135776.1:n.557A=
NR_135779.1:n.557A=
XM_017003807.1:c.-191A= XP_016859296.1:n.-191A=
NM_006588.4:c.130A= MANE Select NP_006579.2:p.Lys44=
NM_001321770.2:c.130A= NP_001308699.1:p.Lys44=
NR_135776.2:n.514A=
NR_135779.2:n.514A=