Canonical Allele Identifier: CA2660578724
Gene: SULT1C4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378364dup , CM000664.2:g.108378364dup GRCh38
NC_000002.11:g.108994820dup , CM000664.1:g.108994820dup GRCh37
NC_000002.10:g.108361252dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.27dup MANE Select ENSP00000272452.2:p.Thr10TyrfsTer3
ENST00000272452.6:c.27dup ENSP00000272452.2:p.Thr10TyrfsTer3
ENST00000409309.3:c.27dup ENSP00000387225.3:p.Thr10TyrfsTer3
ENST00000494122.1:n.454dup
NM_006588.2:c.27dup NP_006579.2:p.Thr10TyrfsTer3
XM_005263919.2:c.27dup XP_005263976.1:p.Thr10TyrfsTer3
NM_001321770.1:c.27dup NP_001308699.1:p.Thr10TyrfsTer3
NM_006588.3:c.27dup NP_006579.2:p.Thr10TyrfsTer3
NR_135776.1:n.454dup
NR_135779.1:n.454dup
NM_006588.4:c.27dup MANE Select NP_006579.2:p.Thr10TyrfsTer3
NM_001321770.2:c.27dup NP_001308699.1:p.Thr10TyrfsTer3
NR_135776.2:n.411dup
NR_135779.2:n.411dup