Canonical Allele Identifier: CA1278109057
Gene: SULT1C4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108387228T= , CM000664.2:g.108387228T= GRCh38
NC_000002.11:g.109003684T= , CM000664.1:g.109003684T= GRCh37
NC_000002.10:g.108370116T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.797-92T= MANE Select ENSP00000272452.2:n.797-92T=
ENST00000272452.6:c.797-92T= ENSP00000272452.2:n.797-92T=
ENST00000409309.3:c.572-92T= ENSP00000387225.3:n.572-92T=
NM_006588.2:c.797-92T= NP_006579.2:n.797-92T=
XM_005263919.2:c.572-92T= XP_005263976.1:n.572-92T=
NM_001321770.1:c.572-92T= NP_001308699.1:n.572-92T=
NM_006588.3:c.797-92T= NP_006579.2:n.797-92T=
NR_135776.1:n.1049-92T=
NR_135779.1:n.778-92T=
XM_017003807.1:c.527-92T= XP_016859296.1:n.527-92T=
NM_006588.4:c.797-92T= MANE Select NP_006579.2:n.797-92T=
NM_001321770.2:c.572-92T= NP_001308699.1:n.572-92T=
NR_135776.2:n.1006-92T=
NR_135779.2:n.735-92T=