Canonical Allele Identifier: CA1278105160
Gene: SULT1C4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378404A= , CM000664.2:g.108378404A= GRCh38
NC_000002.11:g.108994860A= , CM000664.1:g.108994860A= GRCh37
NC_000002.10:g.108361292A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.67A= MANE Select ENSP00000272452.2:p.Lys23=
ENST00000272452.6:c.67A= ENSP00000272452.2:p.Lys23=
ENST00000409309.3:c.67A= ENSP00000387225.3:p.Lys23=
ENST00000494122.1:n.494A=
NM_006588.2:c.67A= NP_006579.2:p.Lys23=
XM_005263919.2:c.67A= XP_005263976.1:p.Lys23=
NM_001321770.1:c.67A= NP_001308699.1:p.Lys23=
NM_006588.3:c.67A= NP_006579.2:p.Lys23=
NR_135776.1:n.494A=
NR_135779.1:n.494A=
NM_006588.4:c.67A= MANE Select NP_006579.2:p.Lys23=
NM_001321770.2:c.67A= NP_001308699.1:p.Lys23=
NR_135776.2:n.451A=
NR_135779.2:n.451A=