Canonical Allele Identifier: CA1278105109
Gene: SULT1C4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378281C= , CM000664.2:g.108378281C= GRCh38
NC_000002.11:g.108994737C= , CM000664.1:g.108994737C= GRCh37
NC_000002.10:g.108361169C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.-57C= MANE Select ENSP00000272452.2:n.-57C=
ENST00000272452.6:c.-57C= ENSP00000272452.2:n.-57C=
ENST00000409309.3:c.-57C= ENSP00000387225.3:n.-57C=
ENST00000494122.1:n.371C=
NM_006588.2:c.-57C= NP_006579.2:n.-57C=
XM_005263919.2:c.-57C= XP_005263976.1:n.-57C=
NM_001321770.1:c.-57C= NP_001308699.1:n.-57C=
NM_006588.3:c.-57C= NP_006579.2:n.-57C=
NR_135776.1:n.371C=
NR_135779.1:n.371C=
NM_006588.4:c.-57C= MANE Select NP_006579.2:n.-57C=
NM_001321770.2:c.-57C= NP_001308699.1:n.-57C=
NR_135776.2:n.328C=
NR_135779.2:n.328C=