Canonical Allele Identifier: CA1278109056
Gene: SULT1C4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108387227A= , CM000664.2:g.108387227A= GRCh38
NC_000002.11:g.109003683A= , CM000664.1:g.109003683A= GRCh37
NC_000002.10:g.108370115A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.797-93A= MANE Select ENSP00000272452.2:n.797-93A=
ENST00000272452.6:c.797-93A= ENSP00000272452.2:n.797-93A=
ENST00000409309.3:c.572-93A= ENSP00000387225.3:n.572-93A=
NM_006588.2:c.797-93A= NP_006579.2:n.797-93A=
XM_005263919.2:c.572-93A= XP_005263976.1:n.572-93A=
NM_001321770.1:c.572-93A= NP_001308699.1:n.572-93A=
NM_006588.3:c.797-93A= NP_006579.2:n.797-93A=
NR_135776.1:n.1049-93A=
NR_135779.1:n.778-93A=
XM_017003807.1:c.527-93A= XP_016859296.1:n.527-93A=
NM_006588.4:c.797-93A= MANE Select NP_006579.2:n.797-93A=
NM_001321770.2:c.572-93A= NP_001308699.1:n.572-93A=
NR_135776.2:n.1006-93A=
NR_135779.2:n.735-93A=