Canonical Allele Identifier: CA1278105097
Gene: SULT1C4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378255A= , CM000664.2:g.108378255A= GRCh38
NC_000002.11:g.108994711A= , CM000664.1:g.108994711A= GRCh37
NC_000002.10:g.108361143A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.-83A= MANE Select ENSP00000272452.2:n.-83A=
ENST00000272452.6:c.-83A= ENSP00000272452.2:n.-83A=
ENST00000409309.3:c.-83A= ENSP00000387225.3:n.-83A=
ENST00000494122.1:n.345A=
NM_006588.2:c.-83A= NP_006579.2:n.-83A=
XM_005263919.2:c.-83A= XP_005263976.1:n.-83A=
NM_001321770.1:c.-83A= NP_001308699.1:n.-83A=
NM_006588.3:c.-83A= NP_006579.2:n.-83A=
NR_135776.1:n.345A=
NR_135779.1:n.345A=
NM_006588.4:c.-83A= MANE Select NP_006579.2:n.-83A=
NM_001321770.2:c.-83A= NP_001308699.1:n.-83A=
NR_135776.2:n.302A=
NR_135779.2:n.302A=